Saturated and unsaturated N-alkamides exhibiting taste and flavor enhancement effect in flavor compositions

ABSTRACT

The present invention is directed to novel compounds and a process for augmenting or imparting a flavor enhancement effect or modifying the perception of one or more of the five basic taste qualities sweet, sour, salt, bitter and umami, to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage, snack, sauce or soup comprising the step of adding to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage, snack, sauce or soup a flavor enhancement or modification of basic taste quality augmenting, enhancing or imparting quantity and concentration of at least one N-substituted unsaturated alkyl amide defined according to the structures:

FIELD OF THE INVENTION

Saturated and unsaturated N-alkamide compounds having sweet, salt or umami taste and flavor enhancement quality.

BACKGROUND OF THE INVENTION

The term Umami, from the Japanese word to describe savory or meaty, is the term used to describe the unique overall fullness, savory or salivatory taste of food. Materials that exhibit this taste quality generally potentate the intensity of glutamate solutions and this is one important characteristic of umami taste. It is increasingly becoming recognized as the fifth sense of taste, the others being sour, sweet, salt and bitter. Compounds traditionally described as possessing this character are monosodium glutamate (MSG), protein hydrolysates, some amino acids and certain nucleotides and phosphates.

MSG is the most widely used material as a ‘taste enhancer’ where it synergizes the perception of ‘savory’ ingredients, but has also been alleged to cause allergic reaction to a proportion of the population.

Among other chemical compounds, several nucleotides have also been described to exhibit the umami effect including Adenosine 5′-(trihydrogen diphosphate), 5′-Cytidylic acid (5′-CMP), 5′-Uridylic acid (5′-UMP), 5′-Adenylic acid (5′-AMP), 5′-Guanylic acid (5′-GMP), 5′-Inosinic acid (5′-IMP) and the di-sodium salts of 5′-Guanylic acid and 5′-Inosinic acid.

Recent literature cites an extensive range of other organic compounds as taste active components of mixtures shown to give the umami taste effect. These include but are not necessarily limited to: organic acids such as succinic acid, lactic acid, saturated straight chain aliphatic acids of six, eight, fourteen, fifteen, sixteen, and seventeen carbon chain lengths, Z4,Z7, Z10,Z13,Z16,Z19-docosahexaenoic acid, Z5,Z8,Z11,Z14,Z17-eicosapentaenoic acid, Z9,Z12, Z16, Z19-octadecadienoic acid, Z9-octadecenoic acid, glutaric acid, adipic acid, suberic acid, and malonic acid. Amino acids having umami effects reported in the literature include glutamic acid, aspartic acid, threonine, alanine, valine, histidine, praline, tyrosine, cystine, methionine, pyroglutamic acid, leucine, lycine, and glycine. Dipeptides possessing umami properties include Val-Glu and Glu-Asp.

Other miscellaneous compounds having umami properties include alpha-amino adipic acid, malic acid, alpha—aminobutyric acid, alpha-aminoisobutyric acid, E2,E4-hexadienal, E2,E4-heptadienal, E2,E4-octadienal, E2,E4-decadienal, Z4-heptenal, E2,Z6-nonadienal, methional, E3,E5-octadien-2-one, 1,6-hexanediamine, tetramethylpyrazine, trimethylpyrazine, cis-6-dodecen-4-olide, glutamate glycoconjugates, fish sauce blended with anchovy paste (U.S. Patent Application 2003/0142090) and a number of naturally occurring amino-acids.

Additionally, a variety of molecules are known by those skilled in the art to provide salt enhancement, these include but are not limited to Adenosine 5′-(trihydrogen diphosphate), 5′-Cytidylic acid (5′-CMP), 5′-Uridylic acid (5′-UMP), 5′-Adenylic acid (5′-AMP), 5′-Guanylic acid (5′-GMP), 5′-Inosinic acid (5′-IMP) and the di-sodium salts of 5′-Guanylic acid and 5′-Inosinic acid, (+)-(S)-Alapyridaine (chemical name N-(1-Carboxyethyl)-6-hydroxymethylpyridinium-3-ol), succinic acid, cetylpyridium chloride, bretylium tosylate, various polypeptides, mixtures of calcium salts of ascorbic acid, potassium chloride, calcium chloride, magnesium chloride, arginine ammonium chloride, alpha-amino acids and their corresponding hydrogen chloride, ammonium and sodium salts and a number of natural plant extracts. Uses of these materials are described in various U.S. Pat. Nos. 4,997,672; 5,288,510; 6,541,050, U.S. Patent Application 2003/0091721 and Eur. Pat. Appl. 2003/1291342.

Additionally, choline chloride has been shown to enhance salt and increase palatability of sodium chloride reduced systems, Physiol Behav. 1994, 55(6), 1039-46.

In addition to this work, our work has included the identification of new flavor materials described in U.S. Ser. No. 10/919,631 filed on Aug. 17, 2004; U.S. Ser. No. 10/861,751 filed on Jun. 4, 2004; and U.S. Ser. No. 10/783,652 filed Feb. 20, 2004.

Despite these disclosures there is an ongoing need for new flavor ingredients particularly those that exhibit advantageous properties for flavor enhancement or modulation, or more preferably the lowering of MSG and/or salt levels in foodstuffs.

SUMMARY OF THE INVENTION

The present invention relates to novel compounds and a process for augmenting or imparting a flavor enhancement effect or modifying the perception of one or more of the five basic taste qualities sweet, sour, salt, bitter and umami, to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage, snack, sauce or soup comprising the step of adding to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage, snack, sauce or soup a flavor enhancement or modification of basic taste quality augmenting, enhancing or imparting quantity and concentration of at least one N-substituted unsaturated alkyl amide defined according to the structures:

where R¹=H or methyl;

-   R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl     and methylene; -   R³ is selected from the group consisting of H, C₁-C₈ straight or     branched chain alkyl, alkenyl, dienalkyl and phenyl; -   or if R¹=H, R² and R³ taken together can represent     cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or     cyclohexenyl; -   or if R¹=Me, R² and R³ taken together can represent     or cyclopropyl, -   R⁴ is selected from the group consisting of H, methyl or ethyl; -   R⁵ is selected from the group consisting of H, methyl and ethyl; -   R⁶ is selected from the group consisting of H, C₁-C₉ straight or     branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no     more than one ring; -   except for in the case of structure 1 when if R⁴=H or methyl and     R⁵=H or methyl, R⁶ as described above and phenyl.

The above formulae define novel compounds with the proviso that in structure 1, if R¹=H and R²=H, then R³ can not be H or methyl unless R⁴=R⁵=H.

As used herein compounds described in structure 2 will be referred to as “cyclopropylic amides”.

A second embodiment relates to novel compounds and a process for augmenting or imparting a flavor enhancement effect or modifying the perception of one or more of the five basic taste qualities sweet, sour, salt, bitter and umami, to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage, snack, sauce or soup comprising the step of adding to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage, snack, sauce or soup a flavor enhancement or modification of basic taste quality augmenting, enhancing or imparting quantity and concentration of at least one N-substituted unsaturated alkyl amide defined according to the structure:

-   -   where R¹=H or methyl;     -   R² is selected from the group consisting of H, C₁-C₄ alkyl,         alkenyl and methylene;     -   R³ is selected from the group consisting of H, C₁-C₈ straight or         branched chain alkyl, alkenyl, dienalkyl and phenyl;     -   or if R¹=H, R² and R³ taken together can represent     -    cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl,         cyclohexyl, or cyclohexenyl;     -   or if R¹=Me, R² and R³ taken together can represent     -    or cyclopropyl,     -   R⁴ is selected from the group consisting of C₁-C₄ alkyl,         alkenyl; removed methylene     -   R⁵ is selected from the group consisting of H, methyl or ethyl;

-   R⁶ is selected from the group consisting of H, methyl and ethyl;

-   R⁷ is selected from the group consisting of H, C₁-C₉ straight or     branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no     more than one ring;     -   except for in the case of structure 3 when if R⁵=H or methyl and         R⁶=H or methyl, R⁷ as described above and phenyl.

A third embodiment relates to novel compounds and a process for augmenting or imparting a flavor enhancement effect or modifying the perception of one or more of the five basic taste qualities sweet, sour, salt, bitter and umami, to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage, snack, sauce or soup comprising the step of adding to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage, snack, sauce or soup a flavor enhancement or modification of basic taste quality augmenting, enhancing or imparting quantity and concentration of at least one N-substituted unsaturated alkyl amide defined according to the structure:

-   -   where R¹=H or methyl;     -   R² is selected from the group consisting of H, C₁-C₄ alkyl,         alkenyl and methylene;     -   R³ is selected from the group consisting of H, C₁-C₈ straight or         branched chain alkyl, alkenyl, dienalkyl and phenyl;     -   or if R¹=H, R² and R³ taken together can represent     -    cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl,         cyclohexyl, or cyclohexenyl;     -   or if R¹=Me, R² and R³ taken together can represent     -    or cyclopropyl,     -   R⁴ is selected from the group consisting of C₁-C₄ alkyl;     -   R⁵ is selected from the group consisting of H, methyl or ethyl;     -   R⁶ is selected from the group consisting of H, methyl and ethyl;     -   R⁷ is selected from the group consisting of H, C₁-C₉ straight or         branched chain alkyl, alkenyl, alkyldienyl, acyclic or         containing no more than one ring;     -   except for in the case of structure 4 when if R⁵=H or methyl and         R⁶=H or methyl, R⁷ as described above and phenyl.

In addition to the novel compounds and the use of the compounds to enhance the taste of foodstuffs by the incorporation of the above ingredients and others set forth in this specification in foodstuff and other materials.

DETAILED DESCRIPTION OF THE INVENTION

The formula set forth above describes a general class of novel materials that we have found to enhance the flavor characteristics of food.

In a more preferred embodiment of the invention the amides have the structure set forth in 1 and 2 with wherein

-   where R¹=H or methyl; -   R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl     and methylene; -   R³ is selected from the group consisting of H, C₁-C₈ straight or     branched chain alkyl, alkenyl, dienalkyl and phenyl; -   or if R¹=H, R² and R³ taken together can represent     cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or     cyclohexenyl; -   or if R¹=Me, R² and R³ taken together can represent     or cyclopropyl, -   R⁴ is selected from the group consisting of H, methyl or ethyl; -   R⁵ is selected from the group consisting of H, methyl and ethyl; -   R⁶ is selected from the group consisting of H, C₁-C₉ straight or     branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no     more than one ring; -   except for in the case of structure 1 when if R⁴=H or methyl and     R⁵=H or methyl, R⁶ as described above and phenyl.

The above compounds of the present invention can be used in accordance with the present method in enhancing the salt and umami effects in foods. The above formulae define novel compounds with the proviso that in structure 1, if R¹=H and R²=H, then R³ can not be H or methyl unless R⁴=R⁵=H.

In a highly preferred embodiment of the invention the amides have the structure set forth below:

-   where R¹=H or methyl; -   R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl     and methylene; -   R³ is selected from the group consisting of H, C₁-C₈ straight or     branched chain alkyl, alkenyl, dienalkyl and phenyl; -   or if R¹=H, R² and R³ taken together can represent     cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or     cyclohexenyl; -   or if R¹=Me, R² and R³ taken together can represent     or cyclopropyl, -   R⁴ is selected from the group consisting of H, methyl or ethyl; -   R⁵ is selected from the group consisting of H, methyl and ethyl; -   R⁶ is selected from the group consisting of H, C₁-C₉ straight or     branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no     more than one ring; -   except for in the case of structure 1 when if R⁴=H or methyl and     R⁵=H or methyl, R⁶ as described above and phenyl.

The above compounds of the present invention can be used in accordance with the present method in enhancing the salt and umami effects in foods. The above formulae define novel compounds with the proviso that in structure 1, if R¹=H and R²=H, then R³ can not be H or methyl unless R⁴=R⁵=H.

As used herein the compounds under structure 1 and formula 1 will be referred to as “alkenylamides”.

In the most preferred embodiment of the invention the amides have the structure set forth below:

-   wherein: R⁷ is selected from the group consisting of H, methyl; -   R⁸ is selected from the group consisting of H or methyl, -   or R⁷ and R⁸ taken together can represent cyclopropyl, -   R⁹ is selected from the group consisting of H or methyl; and -   R¹⁰ is selected from the group consisting of H or methyl.

The above compounds of the present invention can be used in accordance with the present method in enhancing the salt and umami effects in foods. The above compounds are also novel with the proviso that in Formula II, if R⁷=H, then R⁸ can not be H or methyl.

In another preferred embodiment of the invention the amides have the structure set forth below:

-   where R¹=H or methyl; -   R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl     and methylene; -   R³ is selected from the group consisting of H, C₁-C₈ straight or     branched chain alkyl, alkenyl, dienalkyl and phenyl; -   or if R¹=H, R² and R³ taken together can represent     cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or     cyclohexenyl; -   or if R¹=Me, R² and R³ taken together can represent     or cyclopropyl, -   R⁴ is selected from the group consisting of C₁-C₄ alkyl, alkenyl and     methylene; -   R⁵ is selected from the group consisting of H, methyl or ethyl; -   R⁶ is selected from the group consisting of H, methyl and ethyl; -   R⁷ is selected from the group consisting of H, C₁-C₉ straight or     branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no     more than one ring; -   except for in the case of structure 1 when if R⁵=H or methyl and     R⁶=H or methyl, R⁷ as described above and phenyl.

In an additional embodiment of the invention a novel compounds and a process for augmenting or imparting a flavor enhancement effect or modifying the perception of one or more of the five basic taste qualities sweet, sour, salt, bitter and umami, to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage, snack, sauce or soup comprising the step of adding to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage, snack, sauce or soup a flavor enhancement or modification of basic taste quality augmenting, enhancing or imparting quantity and concentration of at least one N-substituted unsaturated alkyl amide defined according to the structure:

-   where R¹=H or methyl; -   R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl     and methylene; -   R³ is selected from the group consisting of H, C₁-C₈ straight or     branched chain alkyl, alkenyl, dienalkyl and phenyl; -   or if R¹=H, R² and R³ taken together can represent     cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or     cyclohexenyl; -   or if R¹=Me, R² and R³ taken together can represent     or cyclopropyl, -   R⁴ is selected from the group consisting of C₁-C₄ alkyl; -   R⁵ is selected from the group consisting of H, methyl or ethyl; -   R⁶ is selected from the group consisting of H, methyl and ethyl; -   R⁷ is selected from the group consisting of H, C₁-C₉ straight or     branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no     more than one ring; -   except for in the case of structure 4 when if R⁵=H or methyl and     R⁶=H or methyl, R⁷ as described above and phenyl.

As used herein the most preferred compounds will be referred to hereinafter as dienalkylamides.

As used throughout the application,

is understood to represent an alkene terminus as depicted in R², R³, R⁷ and R⁸ with an attachment to the alpha carbon of the acid moiety in structures 1, 2, 3, 4, 5 and Formulae I and II set forth in the examples.

Our invention specifically relates to the novel compositions according to the Structure 3 above: Compound Double bond configuration R¹ R² R³ R⁴ R⁵ R⁶ R7 as per drawing H cyclopropyl CH3 H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH2CH3 H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH2CH2CH3 H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Isopropyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl t-butyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Vinyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Allyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH2 Cyclopropyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl butyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Sec-butyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3 H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3CH2 H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3CH2CH2 H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Isopropyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl t-butyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl vinyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl allyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH2 Cyclopropyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl butyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Sec-butyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3 H H

H cyclopropyl CH3CH2 H H

H cyclopropyl CH3CH2CH2 H H

H cyclopropyl Isopropyl H H

H cyclopropyl t-butyl H H

H cyclopropyl vinyl H H

H cyclopropyl allyl H H

H cyclopropyl CH2 Cyclopropyl H H

H cyclopropyl butyl H H

H cyclopropyl Sec-butyl H H

H cyclopropyl CH3 H H

H cyclopropyl CH3CH2 H H

H cyclopropyl CH3CH2CH2 H H

H cyclopropyl Isopropyl H H

H cyclopropyl t-butyl H H

H cyclopropyl vinyl H H

H cyclopropyl allyl H H

H cyclopropyl CH2 Cyclopropyl H H

H cyclopropyl butyl H H

H cyclopropyl Sec-butyl H H

H cyclopropyl CH3 Me H

H cyclopropyl CH3CH2 Me H

H cyclopropyl CH3CH2CH2 Me H

H cyclopropyl Isopropyl Me H

H cyclopropyl t-butyl Me H

H cyclopropyl vinyl Me H

H cyclopropyl allyl Me H

H cyclopropyl CH2 Cyclopropyl Me H

H cyclopropyl butyl Me H

H cyclopropyl Sec-butyl Me H

H cyclopropyl CH3 Me H

H cyclopropyl CH3CH2 Me H

H cyclopropyl CH3CH2CH2 Me H

H cyclopropyl Isopropyl Me H

H cyclopropyl t-butyl Me H

H cyclopropyl Vinyl Me H

H cyclopropyl Allyl Me H

H cyclopropyl CH2 CycloPropyl Me H

H cyclopropyl Butyl Me H

H cyclopropyl Sec-butyl Me H

H cyclopropyl CH3 Me H

H cyclopropyl CH3CH2 Me H

H cyclopropyl CH3CH2CH2 Me H

H cyclopropyl Isopropyl Me H

H cyclopropyl t-butyl Me H

H cyclopropyl vinyl Me H

H cyclopropyl allyl Me H

H cyclopropyl CH2 Cyclopropyl Me H

H cyclopropyl butyl Me H

H cyclopropyl Sec-butyl Me H

H cyclopropyl CH3 H Me

H cyclopropyl CH3CH2 H Me

H cyclopropyl CH3CH2CH2 H Me

H cyclopropyl isopropyl H Me

H cyclopropyl t-butyl H Me

H cyclopropyl vinyl H Me

H cyclopropyl allyl H Me

H cyclopropyl CH2 CycloPropyl H Me

H cyclopropyl butyl H Me

H cyclopropyl Sec-butyl H Me

H cyclopropyl CH3 Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3CH2CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl isopropyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl t-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl vinyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl allyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH2 Cyclopropyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl butyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Sec-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3 Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3CH2CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl isopropyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl t-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl vinyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl allyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH2 Cyclopropyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl butyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Sec-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3 H H

H cyclopropyl CH3CH2 H H

H cyclopropyl CH3CH2CH2 H H

H cyclopropyl isopropyl H H

H cyclopropyl t-butyl H H

H cyclopropyl vinyl H H

H cyclopropyl allyl H H

H cyclopropyl CH2 Cyclopropyl H H

H cyclopropyl butyl H H

H cyclopropyl Sec-butyl H H

H cyclopropyl CH3 H H

H cyclopropyl CH3CH2 H H

H cyclopropyl CH3CH2CH2 H H

H cyclopropyl isopropyl H H

H cyclopropyl t-butyl H H

H cyclopropyl vinyl H H

H cyclopropyl allyl H H

H cyclopropyl CH2 Cyclopropyl H H

H cyclopropyl butyl H H

H cyclopropyl Sec-butyl H H

Me Me CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me Me CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me Me CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me Me isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me allyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me CH2 Cyclopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me butyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me CH3 H Me (CH₃)₂C:CHCH₂CH₂

Me Me CH3CH2 H Me (CH₃)₂C:CHCH₂CH₂

Me Me CH3CH2CH2 H Me (CH₃)₂C:CHCH₂CH₂

Me Me isopropyl H Me (CH₃)₂C:CHCH₂CH₂

Me Me t-butyl H Me (CH₃)₂C:CHCH₂CH₂

Me Me vinyl H Me (CH₃)₂C:CHCH₂CH₂

Me Me allyl H Me (CH₃)₂C:CHCH₂CH₂

Me Me CH2 Cyclopropyl H Me (CH₃)₂C:CHCH₂CH₂

Me Me butyl H Me (CH₃)₂C:CHCH₂CH₂

Me Me Sec-butyl H Me (CH₃)₂C:CHCH₂CH₂

Et H CH3 H Me (CH₃)₂C═CHCH₂CH₂

Et H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Et H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Et H isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Et H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Et H vinyl H Me (CH₃)₂C═CHCH₂CH₂

Et H allyl H Me (CH₃)₂C═CHCH₂CH₂

Et H CH2 Cyclopropyl H Me (CH₃)₂C═CHCH₂CH₂

Et H butyl H Me (CH₃)₂C═CHCH₂CH₂

Et H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Et H CH3 H Me (CH₃)₂C═CHCH₂CH₂

Et H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Et H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Et H isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Et H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Et H vinyl H Me (CH₃)₂C═CHCH₂CH₂

Et H allyl H Me (CH₃)₂C═CHCH₂CH₂

Et H CH2 Cyclopropyl H Me (CH₃)₂C═CHCH₂CH₂

Et H butyl H Me (CH₃)₂C═CHCH₂CH₂

Et H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3 Me H

Me H CH3CH2 Me H

Me H CH3CH2CH2 Me H

Me H isopropyl Me H

Me H t-butyl Me H

Me H vinyl Me H

Me H allyl Me H

Me H CH2 Cyclopropyl Me H

Me H butyl Me H

Me H sec-butyl Me H

Me H CH3 Me H

Me H CH3CH2 Me H

Me H CH3CH2CH2 Me H

Me H isopropyl Me H

Me H t-butyl Me H

Me H vinyl Me H

Me H allyl Me H

Me H CH2 Cyclopropyl Me H

Me H butyl Me H

Me H Sec-butyl Me H

Me H CH3 H Me

Me H CH3CH2 H Me

Me H CH3CH2CH2 H Me

Me H isopropyl H Me

Me H t-butyl H Me

Me H vinyl H Me

Me H allyl H Me

Me H CH2 Cyclopropyl H Me

Me H butyl H Me

Me H Sec-butyl H Me

Me H CH3 H Me

Me H CH3CH2 H Me

Me H CH3CH2CH2 H Me

Me H Isopropyl H Me

Me H t-butyl H Me

Me H Vinyl H Me

Me H Allyl H Me

Me H CH2 Cyclopropyl H Me

Me H Butyl H Me

Me H Sec-butyl H Me

H H CH3 Me H

H H CH3CH2 Me H

H H CH3CH2CH2 Me H

H H Isopropyl Me H

H H t-butyl Me H

H H Vinyl Me H

H H Allyl Me H

H H CH2 CycloPropyl Me H

H H Butyl Me H

H H Sec-butyl Me H

H H CH3 Me H

H H CH3CH2 Me H

H H CH3CH2CH2 Me H

H H Isopropyl Me H

H H t-butyl Me H

H H Vinyl Me H

H H Allyl Me H

H H CH2 CycloPropyl Me H

H H Butyl Me H

H H Sec-butyl Me H

H H CH3 H Me

H H CH3CH2 H Me

H H CH3CH2CH2 H Me

H H Isopropyl H Me

H H t-butyl H Me

H H Vinyl H Me

H H Allyl H Me

H H CH2 CycloPropyl H Me

H H Butyl H Me

H H Sec-butyl H Me

H H CH3 H Me

H H CH3CH2 H Me

H H CH3CH2CH2 H Me

H H Isopropyl H Me

H H t-butyl H Me

H H Vinyl H Me

H H Allyl H Me

H H CH2 Cyclopropyl H Me

H H Butyl H Me

H H Sec-butyl H Me

H H CH3 Me H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H H Isopropyl Me H CH₃CH₂CH═CHCH₂CH₂

H H t-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Vinyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Allyl Me H CH₃CH₂CH═CHCH₂CH₂

H H CH2 CycloPropyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Butyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Sec-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H H CH3 Me H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H H Isopropyl Me H CH₃CH₂CH═CHCH₂CH₂

H H t-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Vinyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Allyl Me H CH₃CH₂CH═CHCH₂CH₂

H H CH2 CycloPropyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Butyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Sec-butyl Me H CH₃CH₂CH═CHCH₂CH₂

Me H CH3 H H

Me H CH3CH2 H H

Me H CH3CH2CH2 H H

Me H Isopropyl H H

Me H t-butyl H H

Me H Vinyl H H

Me H Allyl H H

Me H CH2 CycloPropyl H H

Me H Butyl H H

Me H Sec-butyl H H

Me H CH3 H H

Me H CH3CH2 H H

Me H CH3CH2CH2 H H

Me H Isopropyl H H

Me H t-butyl H H

Me H Vinyl H H

Me H Allyl H H

Me H CH2 CycloPropyl H H

Me H Butyl H H

Me H Sec-butyl H H

H H CH3 H H

H H CH3CH2 H H

H H CH3CH2CH2 H H

Compound Double bond configuration R¹ R² R³ R⁴ R⁵ R⁶ R7 as per drawing H H Isopropyl H H

H H t-butyl H H

H H Vinyl H H

H H Allyl H H

H H CH2 CycloPropyl H H

H H Butyl H H

H H Sec-butyl H H

H H CH3 H H

H H CH3CH2 H H

H H CH3CH2CH2 H H

H H Isopropyl H H

H H t-butyl H H

H H Vinyl H H

H H Allyl H H

H H CH2 cyclopropyl H H

H H Butyl H H

H H Sec-butyl H H

Me Me CH3 H H

Me Me CH3CH2 H H

Me Me CH3CH2CH2 H H

Me Me Isopropyl H H

Me Me t-butyl H H

Me Me Vinyl H H

Me Me Allyl H H

Me Me CH2 Cyclopropyl H H

Me Me Butyl H H

Me Me Sec-butyl H H

Me Me CH3 H H

Me Me CH3CH2 H H

Me Me CH3CH2CH2 H H

Me Me Isopropyl H H

Me Me t-butyl H H

Me Me Vinyl H H

Me Me Allyl H H

Me Me CH2 CycloPropyl H H

Me Me Butyl H H

Me Me Sec-butyl H H

Me H Et CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me H Et CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Et CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Et Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et Vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et Allyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et CH2 CycloPropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et Butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me H Et CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Et CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Et Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et Vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et Allyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et CH2 Cyclopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Et Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl CH3 H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl t-butyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl Vinyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl Allyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl CH2 CycloPropyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl Butyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl CH3 H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl t-butyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl Vinyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl Allyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl CH2 Cyclopropyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl butyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

H Me CH3 H Me (CH₃)₂C═CHCH₂CH₂

H Me CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

H Me CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

H Me Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

H Me t-butyl H Me (CH₃)₂C═CHCH₂CH₂

H Me Vinyl H Me (CH₃)₂C═CHCH₂CH₂

H Me Allyl H Me (CH₃)₂C═CHCH₂CH₂

H Me CH2 CycloPropyl H Me (CH₃)₂C═CHCH₂CH₂

H Me Butyl H Me (CH₃)₂C═CHCH₂CH₂

H Me Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

H Me CH3 H Me (CH₃)₂C═CHCH₂CH₂

H Me CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

H Me CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

H Me Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

H Me t-butyl H Me (CH₃)₂C═CHCH₂CH₂

H Me Vinyl H Me (CH₃)₂C═CHCH₂CH₂

H Me Allyl H Me (CH₃)₂C═CHCH₂CH₂

H Me CH2 Cyclopropyl H Me (CH₃)₂C═CHCH₂CH₂

H Me butyl H Me (CH₃)₂C═CHCH₂CH₂

H Me Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

H

CH3 H Me (CH₃)₂C═CHCH₂CH₂

H

CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

H

CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

H

Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

H

t-butyl H Me (CH₃)₂C═CHCH₂CH₂

H

Vinyl H Me (CH₃)₂C═CHCH₂CH₂

H

Allyl H Me (CH₃)₂C═CHCH₂CH₂

H

CH2 CycloPropyl H Me (CH₃)₂C═CHCH₂CH₂

H

Butyl H Me (CH₃)₂C═CHCH₂CH₂

H

Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

H

CH3 H Me (CH₃)₂C═CHCH₂CH₂

H

CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

H

CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

H

Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

H

t-butyl H Me (CH₃)₂C═CHCH₂CH₂

H

Vinyl H Me (CH₃)₂C═CHCH₂CH₂

H

Allyl H Me (CH₃)₂C═CHCH₂CH₂

H

CH2 Cyclopropyl H Me (CH₃)₂C═CHCH₂CH₂

H

butyl H Me (CH₃)₂C═CHCH₂CH₂

H

Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

H

CH3 H Me (CH₃)₂C═CHCH₂CH₂

H

CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

H

CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

H

Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

H

t-butyl H Me (CH₃)₂C═CHCH₂CH₂

H

Vinyl H Me (CH₃)₂C═CHCH₂CH₂

H

Allyl H Me (CH₃)₂C═CHCH₂CH₂

H

CH2 CycloPropyl H Me (CH₃)₂C═CHCH₂CH₂

H

Butyl H Me (CH₃)₂C═CHCH₂CH₂

H

Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

H

CH3 H Me (CH₃)₂C═CHCH₂CH₂

H

CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

H

CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

H

Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

H

t-butyl H Me (CH₃)₂C═CHCH₂CH₂

H

Vinyl H Me (CH₃)₂C═CHCH₂CH₂

H

Allyl H Me (CH₃)₂C═CHCH₂CH₂

H

CH2 Cyclopropyl H Me (CH₃)₂C═CHCH₂CH₂

H

butyl H Me (CH₃)₂C═CHCH₂CH₂

H

Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl CH3 H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH3CH2 H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH3CH2CH2 H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Isopropyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl t-butyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Vinyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Allyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH2 CycloPropyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Butyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Sec-butyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH3 H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH3CH2 H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH3CH2CH2 H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Isopropyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl t-butyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Vinyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Allyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH2 CycloPropyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Butyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Sec-butyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH3 H Me

H cyclopropyl CH3CH2 H Me

H cyclopropyl CH3CH2CH2 H Me

H cyclopropyl Isopropyl H Me

H cyclopropyl t-butyl H Me

H cyclopropyl Vinyl H Me

H cyclopropyl Allyl H Me

H cyclopropyl CH2 CycloPropyl H Me

H cyclopropyl Butyl H Me

H cyclopropyl Sec-butyl H Me

H cyclopropyl CH3 H Me

H cyclopropyl CH3CH2 H Me

H cyclopropyl CH3CH2CH2 H Me

H cyclopropyl Isopropyl H Me

H cyclopropyl t-butyl H Me

H cyclopropyl Vinyl H Me

H cyclopropyl Allyl H Me

H cyclopropyl CH2 CycloPropyl H Me

H cyclopropyl Butyl H Me

H cyclopropyl Sec-butyl H Me

H cyclopropyl CH3 H Me Me

H cyclopropyl CH3CH2 H Me Me

H cyclopropyl CH3CH2CH2 H Me Me

H cyclopropyl Isopropyl H Me Me

H cyclopropyl t-butyl H Me Me

H cyclopropyl Vinyl H Me Me

H cyclopropyl Allyl H Me Me

H cyclopropyl CH2 CycloPropyl H Me Me

H cyclopropyl Butyl H Me Me

H cyclopropyl Sec-butyl H Me Me

H cyclopropyl CH3 H H

H cyclopropyl CH3CH2 H H

H cyclopropyl CH3CH2CH2 H H

H cyclopropyl Isopropyl H H

H cyclopropyl t-butyl H H

H cyclopropyl Vinyl H H

H cyclopropyl Allyl H H

H cyclopropyl CH2 CycloPropyl H H

H cyclopropyl Butyl H H

H cyclopropyl Sec-butyl H H

H cyclopropyl CH3 H H

H cyclopropyl CH3CH2 H H

H cyclopropyl CH3CH2CH2 H H

H cyclopropyl Isopropyl H H

H cyclopropyl t-butyl H H

H cyclopropyl Vinyl H H

H cyclopropyl Allyl H H

H cyclopropyl CH2 CycloPropyl H H

H cyclopropyl Butyl H H

H cyclopropyl Sec-butyl H H

H H CH3 H Me

H H CH3CH2 H Me

H H CH3CH2CH2 H Me

H H Isopropyl H Me

H H t-butyl H Me

H H Vinyl H Me

H H Allyl H Me

H H CH2 CycloPropyl H Me

H H Butyl H Me

H H Sec-butyl H Me

H H CH3 H Me

H H CH3CH2 H Me

H H CH3CH2CH2 H Me

H H Isopropyl H Me

H H t-butyl H Me

H H Vinyl H Me

H H Allyl H Me

H H CH2 CycloPropyl H Me

H H Butyl H Me

H H Sec-butyl H Me

H H CH3 H H

H H CH3CH2 H H

H H CH3CH2CH2 H H

H H Isopropyl H H

H H t-butyl H H

H H Vinyl H H

H H Allyl H H

H H CH2 CycloPropyl H H

H H Butyl H H

H H Sec-butyl H H

H H CH3 H H

H H CH3CH2 H H

H H CH3CH2CH2 H H

H H Isopropyl H H

H H t-butyl H H

H H Vinyl H H

H H Allyl H H

H H CH2 CycloPropyl H H

H H Butyl H H

H H Sec-Butyl H H

Me H CH3 H H CH₃CH₂CH═CHCH₂CH₂

Me H CH3CH2 H H CH₃CH₂CH═CHCH₂CH₂

Me H CH3CH2CH2 H H CH₃CH₂CH═CHCH₂CH₂

Me H Isopropyl H H CH₃CH₂CH═CHCH₂CH₂

Me H t-butyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Vinyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Allyl H H CH₃CH₂CH═CHCH₂CH₂

Me H CH2 Cyclopropyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Butyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Sec-butyl H H CH₃CH₂CH═CHCH₂CH₂

Me H CH3 H H CH₃CH₂CH═CHCH₂CH₂

Me H CH3CH2 H H CH₃CH₂CH═CHCH₂CH₂

Me H CH3CH2CH2 H H CH₃CH₂CH═CHCH₂CH₂

Me H Isopropyl H H CH₃CH₂CH═CHCH₂CH₂

Me H t-butyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Vinyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Allyl H H CH₃CH₂CH═CHCH₂CH₂

Me H CH2 Cyclopropyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Butyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Sec-butyl H H CH₃CH₂CH═CHCH₂CH₂

H H CH3 H H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2 H H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2CH2 H H CH₃CH₂CH═CHCH₂CH₂

H H Isopropyl H H CH₃CH₂CH═CHCH₂CH₂

H H t-butyl H H CH₃CH₂CH═CHCH₂CH₂

H H Vinyl H H CH₃CH₂CH═CHCH₂CH₂

H H Allyl H H CH₃CH₂CH═CHCH₂CH₂

H H CH2 Cyclopropyl H H CH₃CH₂CH═CHCH₂CH₂

H H Butyl H H CH₃CH₂CH═CHCH₂CH₂

H H Sec-butyl H H CH₃CH₂CH═CHCH₂CH₂

H H CH3 H H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2 H H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2CH2 H H CH₃CH₂CH═CHCH₂CH₂

H H Isopropyl H H CH₃CH₂CH═CHCH₂CH₂

H H t-butyl H H CH₃CH₂CH═CHCH₂CH₂

H H Vinyl H H CH₃CH₂CH═CHCH₂CH₂

H H Allyl H H CH₃CH₂CH═CHCH₂CH₂

H H CH Cyclopropyl H H CH₃CH₂CH═CHCH₂CH₂

H H Butyl H H CH₃CH₂CH═CHCH₂CH₂

H H Sec-butyl H H CH₃CH₂CH═CHCH₂CH₂

Our invention specifically relates to the novel compositions according to the formula I above: Compound Double bond configuration R¹ R² R³ R⁴ R⁵ R⁶ as per drawing H

H Me (CH₃)₂C═CHCH₂CH₂

H

H Me (CH₃)₂C═CHCH₂CH₂

H

H Me (CH₃)₂C═CHCH₂CH₂

H

H Me (CH₃)₂C═CHCH₂CH₂

H

H Me (CH₃)₂C═CHCH₂CH₂

H

H Me (CH₃)₂C═CHCH₂CH₂

H

H H CH₃CH₂CH═CHCH₂CH₂

H

H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl H H

H cyclopropyl H H

H cyclopropyl H H

H cyclopropyl Me H

Me H H H Me

H H H H Me

H H H H Me

H H H Me H CH₃CH₂CH═CHCH₂CH₂

H H H Me H CH₃CH₂CH═CHCH₂CH₂

H H Me H H

H H Me H H

H H H H H

H H H H H

Me Me Me H H

Me Me Me H H

Me H Et H Me (CH₃)₂C═CHCH₂CH₂

Me H Et H Me (CH₃)₂C═CHCH₂CH₂

Refering to Formula II above, the present invention relates to the novel compositions according to the formula II above: Geranyl 2,3-double R⁷ R⁸ R⁹ R¹⁰ Bond configuration Compound Cyclopropyl Me Me E

Cyclopropyl Me Me Z

Me Me Me Me E

Me Me Me Me Z

Me Me E

Me Me Z

Me Me E

Me Me Z

These compounds and uses thereof have been found beneficial in augmenting or imparting an olfactory effect taste enhancement or somatosensory effect to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage, snack, sauce or soup particularly providing a (a) umami taste, (b) salt effects, (c) flavor enhancement, and (d) preferred overall flavor profile.

More specifically, examples of the organoleptic properties for the dienalkylamides of our invention are as follows:

Relating to Formula I R¹ R² R³ R⁴ R⁵ R⁶ Compound Taste profile H cyclopropyl H H CH₃CH₂CH═CHCH₂CH₂

Moderate Umami, off fish oily character H cyclopropyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

Oily, moderate umami H H H Me H CH₃CH₂CH═CHCH₂CH₂

Potent warming at 10 ppm

Relating to Formula II R⁷ R⁸ R⁹ R¹⁰ Compound Taste profile Cyclopropyl Me Me

Salt, MSG, Umami, mouthfeel, lasting sweetness. Cyclopropyl Me Me

Salty, MSG, Umami, brothy, mouthfeel, sweetness. Me Me Me Me

Some salt enhancement, umami and strong MSG effect, sweet end profile Me Me Me Me

Salt enhancement, MSG enhancement, Umami, brothy, sweet end profile

Me Me

Moderate umami, salt like, lemon character.

Me Me

Moderate umami, some saltiness.

Me Me

Clean, weak umami effect at 10 ppm

Me Me

Clean, weak umami effect at 10 ppm

Relating to Structure 3 R¹ R²r³ R⁴ R⁵ R⁶ R⁷ Compound Taste profile H Cyclopropyl Et H Me (CH₃)₂C═CHCH₂CH₂ Weak salt and Umami

Other novel compounds of the present invention include the following according to Structure 1 above: Compound Double bond R1 R2 R3 R4 R5 R6 configuration as per drawing H cyclopropyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl H Me

H cyclopropyl H Me

H cyclopropyl H Me Me

H cyclopropyl H Me

H cyclopropyl H Me

H cyclopropyl H H

H cyclopropyl H H

H H H H Me

H H H H Me

H H H H Me

H H H H Me

H H H H H

H H H H H

Me

H Me (CH₃)₂C═CH CH₂CH₂

Other compounds of the present invention include the following according to Structure 2 above: R1 R2 R3 R4 R5 R6 Compound H cyclopropyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl H H CH₃CH₂CH═CHCH₂CH₂

H

H Me (CH₃)₂C═CHCH₂CH₂

H H H H Me (CH₃)₂C═CHCH₂CH₂

H H Me H Me (CH₃)₂C═CHCH₂CH₂

H Me Me H Me (CH₃)₂C═CHCH₂CH₂

Other compounds of the present invention include the following according to Structure 4 above: Compound Double bond configuration R¹ R² R³ R⁴ R⁵ R⁶ R7 as per drawing H cyclopropyl CH3 H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH2CH3 H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH2CH2CH3 H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Isopropyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl t-butyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Vinyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Allyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH2 Cyclopropyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl butyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Sec-butyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3 H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3CH2 H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3CH2CH2 H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Isopropyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl t-butyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl vinyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl allyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH2 Cyclopropyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl butyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Sec-butyl H H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3 H H

H cyclopropyl CH3CH2 H H

H cyclopropyl CH3CH2CH2 H H

H cyclopropyl Isopropyl H H

H cyclopropyl t-butyl H H

H cyclopropyl vinyl H H

H cyclopropyl allyl H H

H cyclopropyl CH2 Cyclopropyl H H

H cyclopropyl butyl H H

H cyclopropyl Sec-butyl H H

H cyclopropyl CH3 H H

H cyclopropyl CH3CH2 H H

H cyclopropyl CH3CH2CH2 H H

H cyclopropyl Isopropyl H H

H cyclopropyl t-butyl H H

H cyclopropyl vinyl H H

H cyclopropyl allyl H H

H cyclopropyl CH2 Cyclopropyl H H

H cyclopropyl butyl H H

H cyclopropyl Sec-butyl H H

H cyclopropyl CH3 Me H

H cyclopropyl CH3CH2 Me H

H cyclopropyl CH3CH2CH2 Me H

H cyclopropyl Isopropyl Me H

H cyclopropyl t-butyl Me H

H cyclopropyl vinyl Me H

H cyclopropyl allyl Me H

H cyclopropyl CH2 Cyclopropyl Me H

H cyclopropyl butyl Me H

H cyclopropyl Sec-butyl Me H

H cyclopropyl CH3 Me H

H cyclopropyl CH3CH2 Me H

H cyclopropyl CH3CH2CH2 Me H

H cyclopropyl Isopropyl Me H

H cyclopropyl t-butyl Me H

H cyclopropyl Vinyl Me H

H cyclopropyl Allyl Me H

H cyclopropyl CH2 CycloPropyl Me H

H cyclopropyl Butyl Me H

H cyclopropyl Sec-butyl Me H

H cyclopropyl CH3 H Me

H cyclopropyl CH3CH2 H Me

H cyclopropyl CH3CH2CH2 H Me

H cyclopropyl isopropyl H Me

H cyclopropyl t-butyl H Me

H cyclopropyl vinyl H Me

H cyclopropyl allyl H Me

H cyclopropyl CH2 Cyclopropyl H Me

H cyclopropyl butyl H Me

H cyclopropyl Sec-butyl H Me

H cyclopropyl CH3 H Me

H cyclopropyl CH3CH2 H Me

H cyclopropyl CH3CH2CH2 H Me

H cyclopropyl isopropyl H Me

H cyclopropyl t-butyl H Me

H cyclopropyl vinyl H Me

H cyclopropyl allyl H Me

H cyclopropyl CH2 CycloPropyl H Me

H cyclopropyl butyl H Me

H cyclopropyl Sec-butyl H Me

H cyclopropyl CH3 Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3CH2CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl isopropyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl t-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl vinyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl allyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH2 Cyclopropyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl butyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Sec-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3 Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3CH2CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl isopropyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl t-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl vinyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl allyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH2 Cyclopropyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl butyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl Sec-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H cyclopropyl CH3 H H

H cyclopropyl CH3CH2 H H

H cyclopropyl CH3CH2CH2 H H

H cyclopropyl isopropyl H H

H cyclopropyl t-butyl H H

H cyclopropyl vinyl H H

H cyclopropyl allyl H H

H cyclopropyl CH2 Cyclopropyl H H

H cyclopropyl butyl H H

H cyclopropyl Sec-butyl H H

H cyclopropyl CH3 H H

H cyclopropyl CH3CH2 H H

H cyclopropyl CH3CH2CH2 H H

H cyclopropyl isopropyl H H

H cyclopropyl t-butyl H H

H cyclopropyl vinyl H H

H cyclopropyl allyl H H

H cyclopropyl CH2 Cyclopropyl H H

H cyclopropyl butyl H H

H cyclopropyl Sec-butyl H H

Me Me CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me Me CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me Me CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me Me isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me allyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me CH2 Cyclopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me butyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me Me CH3 H Me (CH₃)₂C:CHCH₂CH₂

Me Me CH3CH2 H Me (CH₃)₂C:CHCH₂CH₂

Me Me CH3CH2CH2 H Me (CH₃)₂C:CHCH₂CH₂

Me Me isopropyl H Me (CH₃)₂C:CHCH₂CH₂

Me Me t-butyl H Me (CH₃)₂C:CHCH₂CH₂

Me Me vinyl H Me (CH₃)₂C:CHCH₂CH₂

Me Me allyl H Me (CH₃)₂C:CHCH₂CH₂

Me Me CH2 Cyclopropyl H Me (CH₃)₂C:CHCH₂CH₂

Me Me butyl H Me (CH₃)₂C:CHCH₂CH₂

Me Me Sec-butyl H Me (CH₃)₂C:CHCH₂CH₂

H H CH3 H Me (CH₃)₂C═CHCH₂CH₂

H H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

H H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

H H isopropyl H Me (CH₃)₂C═CHCH₂CH₂

H H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

H H vinyl H Me (CH₃)₂C═CHCH₂CH₂

H H allyl H Me (CH₃)₂C═CHCH₂CH₂

H H CH2 Cyclopropyl H Me (CH₃)₂C═CHCH₂CH₂

H H butyl H Me (CH₃)₂C═CHCH₂CH₂

H H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

H H CH3 H Me (CH₃)₂C═CHCH₂CH₂

H H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

H H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

H H isopropyl H Me (CH₃)₂C═CHCH₂CH₂

H H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

H H vinyl H Me (CH₃)₂C═CHCH₂CH₂

H H allyl H Me (CH₃)₂C═CHCH₂CH₂

H H CH2 Cyclopropyl H Me (CH₃)₂C═CHCH₂CH₂

H H butyl H Me (CH₃)₂C═CHCH₂CH₂

H H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3 Me H

Me H CH3CH2 Me H

Me H CH3CH2CH2 Me H

Me H isopropyl Me H

Me H t-butyl Me H

Me H vinyl Me H

Me H allyl Me H

Me H CH2 Cyclopropyl Me H

Me H butyl Me H

Me H sec-butyl Me H

Me H CH3 Me H

Me H CH3CH2 Me H

Me H CH3CH2CH2 Me H

Me H isopropyl Me H

Me H t-butyl Me H

Me H vinyl Me H

Me H allyl Me H

Me H CH2 Cyclopropyl Me H

Me H butyl Me H

Me H Sec-butyl Me H

Me H CH3 H Me

Me H CH3CH2 H Me

Me H CH3CH2CH2 H Me

Me H isopropyl H Me

Me H t-butyl H Me

Me H vinyl H Me

Me H allyl H Me

Me H CH2 Cyclopropyl H Me

Me H butyl H Me

Me H Sec-butyl H Me

Me H CH3 H Me

Me H CH3CH2 H Me

Me H CH3CH2CH2 H Me

Me H Isopropyl H Me

Me H t-butyl H Me

Me H Vinyl H Me

Me H Allyl H Me

Me H CH2 CycloPropyl H Me

Me H Butyl H Me

Me H Sec-butyl H Me

H H CH3 Me H

H H CH3CH2 Me H

H H CH3CH2CH2 Me H

H H Isopropyl Me H

H H t-butyl Me H

H H Vinyl Me H

H H Allyl Me H

H H CH2 CycloPropyl Me H

H H Butyl Me H

H H Sec-butyl Me H

H H CH3 Me H

H H CH3CH2 Me H

H H CH3CH2CH2 Me H

H H Isopropyl Me H

H H t-butyl Me H

H H Vinyl Me H

H H Allyl Me H

H H CH2 CycloPropyl Me H

H H Butyl Me H

H H Sec-butyl Me H

H H CH3 H Me

H H CH3CH2 H Me

H H CH3CH2CH2 H Me

H H Isopropyl H Me

H H t-butyl H Me

H H Vinyl H Me

H H Allyl H Me

H H CH2 CycloPropyl H Me

H H Butyl H Me

H H Sec-butyl H Me

H H CH3 H Me

H H CH3CH2 H Me

H H CH3CH2CH2 H Me

H H Isopropyl H Me

H H t-butyl H Me

H H Vinyl H Me

H H Allyl H Me

H H CH2 CycloPropyl H Me

H H Butyl H Me

H H Sec-butyl H Me

H H CH3 Me H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H H Isopropyl Me H CH₃CH₂CH═CHCH₂CH₂

H H t-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Vinyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Allyl Me H CH₃CH₂CH═CHCH₂CH₂

H H CH2 CycloPropyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Butyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Sec-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H H CH3 Me H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2CH2 Me H CH₃CH₂CH═CHCH₂CH₂

H H Isopropyl Me H CH₃CH₂CH═CHCH₂CH₂

H H t-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Vinyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Allyl Me H CH₃CH₂CH═CHCH₂CH₂

H H CH2 CycloPropyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Butyl Me H CH₃CH₂CH═CHCH₂CH₂

H H Sec-butyl Me H CH₃CH₂CH═CHCH₂CH₂

H H CH3 H H

H H CH3CH2 H H

H H CH3CH2CH2 H H

H H Isopropyl H H

H H t-butyl H H

H H Vinyl H H

H H Allyl H H

H H CH2 CycloPropyl H H

H H Butyl H H

H H Sec-butyl H H

H H CH3 H H

H H CH3CH2 H H

H H CH3CH2CH2 H H

H H Isopropyl H H

H H t-butyl H H

H H Vinyl H H

H H Allyl H H

H H CH2 CycloPropyl H H

H H Butyl H H

H H Sec-butyl H H

H H CH3 H H

H H CH3CH2 H H

H H CH3CH2CH2 H H

H H Isopropyl H H

H H t-butyl H H

H H Vinyl H H

H H Allyl H H

H H CH2 CycloPropyl H H

H H Butyl H H

H H Sec-butyl H H

H H CH3 H H

H H CH3CH2 H H

H H CH3CH2CH2 H H

H H Isopropyl H H

Compound Double bond R¹ R² R³ R⁴ R⁵ R⁶ R⁷ configuration as per drawing H H t-butyl H H

H H Vinyl H H

H H Allyl H H

H H CH2 cyclo-propyl H H

H H Butyl H H

H H Sec-butyl H H

Me Me CH3 H H

Me Me CH3CH2 H H

Me Me CH3CH2CH2 H H

Me Me Isopropyl H H

Me Me t-butyl H H

Me Me Vinyl H H

Me Me Allyl H H

Me Me CH2 Cyclo-Propyl H H

Me Me Butyl H H

Me Me Sec-butyl H H

Me Me CH3 H H

Me Me CH3CH2 H H

Me Me CH3CH2CH2 H H

Me Me Isopropyl H H

Me Me t-butyl H H

Me Me Vinyl H H

Me Me Allyl H H

Me Me CH2 Cyclo-Propyl H H

Me Me Butyl H H

Me Me Sec-butyl H H

Me H CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Allyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH2 Cyclo-Propyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Allyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH2 Cyclo-Propyl H Me (CH₃)₂C═CHCH₂CH₂

Me H butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Allyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH2 Cyclo-Propyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Allyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH2 Cyclo-Propyl H Me (CH₃)₂C═CHCH₂CH₂

Me H butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Allyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH2 Cyclo-Propyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Allyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH2 Cyclo-Propyl H Me (CH₃)₂C═CHCH₂CH₂

Me H butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Allyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH2 Cyclo-Propyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Allyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH2 Cyclo-Propyl H Me (CH₃)₂C═CHCH₂CH₂

Me H butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Allyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH2 Cyclo-Propyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H CH3CH2CH2 H Me (CH₃)₂C═CHCH₂CH₂

Me H Isopropyl H Me (CH₃)₂C═CHCH₂CH₂

Me H t-butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Vinyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Allyl H Me (CH₃)₂C═CHCH₂CH₂

Me H CH2 Cyclo-Propyl H Me (CH₃)₂C═CHCH₂CH₂

Me H butyl H Me (CH₃)₂C═CHCH₂CH₂

Me H Sec-butyl H Me (CH₃)₂C═CHCH₂CH₂

H cyclopropyl CH3 H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH3CH2 H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH3CH2CH2 H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Isopropyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl t-butyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Vinyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Allyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH2 Cyclo-Propyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Butyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Sec-butyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH3 H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH3CH2 H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH3CH2CH2 H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Isopropyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl t-butyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Vinyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Allyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH2 Cyclo-Propyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Butyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl Sec-butyl H H CH₃(CH₂)₄CH═CHCH₂CH₂

H cyclopropyl CH3 H Me

H cyclopropyl CH3CH2 H Me

H cyclopropyl CH3CH2CH2 H Me

H cyclopropyl Isopropyl H Me

H cyclopropyl t-butyl H Me

H cyclopropyl Vinyl H Me

H cyclopropyl Allyl H Me

H cyclopropyl CH2 Cyclo-Propyl H Me

H cyclopropyl Butyl H Me

H cyclopropyl Sec-butyl H Me

H cyclopropyl CH3 H Me

H cyclopropyl CH3CH2 H Me

H cyclopropyl CH3GH2CH2 H Me

H cyclopropyl Isopropyl H Me

H cyclopropyl t-butyl H Me

H cyclopropyl Vinyl H Me

H cyclopropyl Allyl H Me

H cyclopropyl CH2 Cyclo-Propyl H Me

H cyclopropyl Butyl H Me

H cyclopropyl Sec-butyl H Me

H cyclopropyl CH3 H Me Me

H cyclopropyl CH3CH2 H Me Me

H cyclopropyl CH3CH2CH2 H Me Me

H cyclopropyl Isopropyl H Me Me

H cyclopropyl t-butyl H Me Me

H cyclopropyl Vinyl H Me Me

H cyclopropyl Allyl H Me Me

H cyclopropyl CH2 Cyclo-Propyl H Me Me

H cyclopropyl Butyl H Me Me

H cyclopropyl Sec-butyl H Me Me

H cyclopropyl CH3 H H

H cyclopropyl CH3CH2 H H

H cyclopropyl CH3CH2CH2 H H

H cyclopropyl Isopropyl H H

H cyclopropyl t-butyl H H

H cyclopropyl Vinyl H H

H cyclopropyl Allyl H H

H cyclopropyl CH2 Cyclo-Propyl H H

H cyclopropyl Butyl H H

H cyclopropyl Sec-butyl H H

H cyclopropyl CH3 H H

H cyclopropyl CH3CH2 H H

H cyclopropyl CH3CH2CH2 H H

H cyclopropyl Isopropyl H H

H cyclopropyl t-butyl H H

H cyclopropyl Vinyl H H

H cyclopropyl Allyl H H

H cyclopropyl CH2 Cyclo-Propyl H H

H cyclopropyl Butyl H H

H cyclopropyl Sec-butyl H H

H H CH3 H Me

H H CH3CH2 H Me

H H CH3CH2CH2 H Me

H H Isopropyl H Me

H H t-butyl H Me

H H Vinyl H Me

H H Allyl H Me

H H CH2 Cyclo-Propyl H Me

H H Butyl H Me

H H Sec-butyl H Me

H H CH3 H Me

H H CH3CH2 H Me

H H CH3CH2CH2 H Me

H H Isopropyl H Me

H H t-butyl H Me

H H Vinyl H Me

H H Allyl H Me

H H CH2 Cyclo-Propyl H Me

H H Butyl H Me

H H Sec-butyl H Me

H H CH3 H H

H H CH3CH2 H H

H H CH3CH2CH2 H H

H H Isopropyl H H

H H t-butyl H H

H H Vinyl H H

H H Allyl H H

H H CH2 Cyclo-Propyl H H

H H Butyl H H

H H Sec-butyl H H

H H CH3 H H

H H CH3CH2 H H

H H CH3CH2CH2 H H

H H Isopropyl H H

H H t-butyl H H

H H Vinyl H H

H H Allyl H H

H H CH2 Cyclo-Propyl H H

H H Butyl H H

H H Sec-Butyl H H

Me H CH3 H H CH₃CH₂CH═CHCH₂CH₂

Me H CH3CH2 H H CH₃CH₂CH═CHCH₂CH₂

Me H CH3CH2CH2 H H CH₃CH₂CH═CHCH₂CH₂

Me H Isopropyl H H CH₃CH₂CH═CHCH₂CH₂

Me H t-butyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Vinyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Allyl H H CH₃CH₂CH═CHCH₂CH₂

Me H CH2 Cyclo-Propyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Butyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Sec-butyl H H CH₃CH₂CH═CHCH₂CH₂

Me H CH3 H H CH₃CH₂CH═CHCH₂CH₂

Me H CH3CH2 H H CH₃CH₂CH═CHCH₂CH₂

Me H CH3CH2CH2 H H CH₃CH₂CH═CHCH₂CH₂

Me H Isopropyl H H CH₃CH₂CH═CHCH₂CH₂

Me H t-butyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Vinyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Allyl H H CH₃CH₂CH═CHCH₂CH₂

Me H CH2 Cyclo-Propyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Butyl H H CH₃CH₂CH═CHCH₂CH₂

Me H Sec-butyl H H CH₃CH₂CH═CHCH₂CH₂

H H CH3 H H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2 H H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2CH2 H H CH₃CH₂CH═CHCH₂CH₂

H H Isopropyl H H CH₃CH₂CH═CHCH₂CH₂

H H t-butyl H H CH₃CH₂CH═CHCH₂CH₂

H H Vinyl H H CH₃CH₂CH═CHCH₂CH₂

H H Allyl H H CH₃CH₂CH═CHCH₂CH₂

H H CH2 Cyclo-Propyl H H CH₃CH₂CH═CHCH₂CH₂

H H Butyl H H CH₃CH₂CH═CHCH₂CH₂

H H Sec-butyl H H CH₃CH₂CH═CHCH₂CH₂

H H CH3 H H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2 H H CH₃CH₂CH═CHCH₂CH₂

H H CH3CH2CH2 H H CH₃CH₂CH═CHCH₂CH₂

H H Isopropyl H H CH₃CH₂CH═CHCH₂CH₂

H H t-butyl H H CH₃CH₂CH═CHCH₂CH₂

H H Vinyl H H CH₃CH₂CH═CHCH₂CH₂

H H Allyl H H CH₃CH₂CH═CHCH₂CH₂

H H CH2 Cyclo-Propyl H H CH₃CH₂CH═CHCH₂CH₂

H H Butyl H H CH₃CH₂CH═CHCH₂CH₂

H H Sec-butyl H H CH₃CH₂CH═CHCH₂CH₂

Other compounds of the present invention include the following according to Structure 5 above: Compound Double bond configuration R¹ R² R³ R⁴ R⁵ R⁶ R7 as per drawing H cyclopropyl H H Me (CH₃)₂C═CHCH₂CH₂

H H CH═CH₂ H H Me (CH₃)₂C═CHCH₂CH₂

H H CH(CH₃)₂ H H Me (CH₃)₂C═CHCH₂CH₂

H H H H H Me (CH₃)₂C═CHCH₂CH₂

H H Me H H Me (CH₃)₂C═CHCH₂CH₂

H Me Me H H Me (CH₃)₂C═CHCH₂CH₂

H Cyclopropyl H H H CH₃CH₂CH═CHCH₂CH₂

H H H Me H H CH₃CH₂CH═CHCH₂CH₂

The following compounds and Chemical Abstract (CA) names are provided for various compounds of the present invention. Compound # Structure (Novel compounds) CA Index Name 1

2,6-nonadienamide, N-[(2E)-3,7- dimethyl-2,6-octadienyl]-, (2E,6Z)- 2

2,6-nonadienamide, N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-, (2E,6Z)- 3

2,6-octadienamide, N-[(2E)-3,7- dimethyl-2,6-octadienyl]-3,7- dimethyl-, (2E)- 4

2,6-octadienamide, N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-3,7- dimethyl-, (2E)- 5

2,6-octadienamide, N-[(2E)-3,7- dimethyl-2,6-octadienyl]-3,7- dimethyl-, (2Z)- 6

2,6-octadienamide, N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-3,7- dimethyl-, (2Z)- 7

2,6-octadienamide, 3,7-dimethyl-N- [(2Z,6Z)-2,6-nonadienyl]-, (2E)- 8

2,6-octadienamide, 3,7-dimethyl-N- [(2Z,6Z)-2,6-nonadienyl]-, (2Z)- 9

Cyclopropanecarboxamide, N- [(2Z,6Z)-2,6-nonadienyl]- 10

Cyclopropanecarboxamide, N- [(2E,6Z)-2,6-nonadienyl]- 11

Cyclopropanecarboxamide, N-[(2E)-3- (3-cyclohexen-1-yl)-2-propenyl]- 12

Cyclopropanecarboxamide, N-[(2Z)-3- (3-cyclohexen-1-yl)-2-propenyl]- 13

Cyclopropanecarboxamide, N-[(2E)-2- methyl-3-phenyl-2-propenyl]- 14

Cyclopropanecarboxamide, N-[(2Z)-2- methyl-3-phenyl-2-propenyl]- 15

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-butenyl]- 16

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-butenyl]- 17

Cyclopropanecarboxamide, N- [(2Z,6Z)-2-methyl-2,6-nonadienyl]- 18

Cyclopropanecarboxamide, N- [(2E,6Z)-2-methyl-2,6-nonadienyl]- 19

Cyclopropanecarboxamide, N-[(2E)- 3-phenyl-2-propenyl]- 20

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-propenyl]- 21

Propanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-2,2-dimethyl- 22

Propanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-2,2-dimethyl- 23

Butanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]- 24

Butanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]- 25

Propanamide, N-[(2E)-2-methyl-3- phenyl-2-propenyl]- 26

Propanamide, N-[(2Z)-2-methyl-3- phenyl-2-propenyl]- 27

Propanamide, N-[(2E)-3-phenyl-2- butenyl]- 28

Propanamide, N-[(2Z)-3-phenyl-2- butenyl]- 29

Acetamide, N-[(2E)-2-methyl-3- phenyl-2-propenyl]- 30

Acetamide, N-[(2Z)-2-methyl-3- phenyl-2-propenyl]- 31

Acetamide, N-[(2E)-3-phenyl-2- butenyl]- 32

Acetamide, N-[(2Z)-3-phenyl-2- butenyl]- 33

Acetamide, N-[(2Z,6Z)-2-methyl-2,6- nonadienyl]- 34

Acetamide, N-[(2E,6Z)-2-methyl-2,6- nonadienyl]- 35

Propanamide, N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]- 36

Propanamide, N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]- 37

Acetamide, N-[(2E)-3-(3-cyclohexen- 1-yl)-2-propenyl]- 38

Acetamide, N-[(2Z)-3-(3-cyclohexen- 1-yl)-2-propenyl]- 39

Propanamide, N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]-2,2- dimethyl- 40

Propanamide, N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]-2,2- dimethyl- 41

Butanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-2-methyl- 42

Butanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-2-methyl- 43

Cyclopropanecarboxamide, N-[(2E)- 3,7-dimethyl-2,6-octadienyl]- 44

Cyclopropanecarboxamide, N-[(2Z)- 3,7-dimethyl-2,6-octadienyl]- 45

Propanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-2-methyl- 46

Propanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-2-methyl- 47

2-butenamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-, (2E)- 48

2-butenamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-, (2E)- 49

2-butenamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-3-methyl- 50

2-butenamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-3-methyl- 51

Cyclopropanecarboxamide, N- [(2E,6Z)-2,6-dodecadienyl]- 52

Cyclopropanecarboxamide, N-[(2E)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]- 53

Cyclopropanecarboxamide, N-[(2Z)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]- 54

Cyclopropanecarboxamide, N-(3- methyl-2-butenyl)- 55

Cyclopropanecarboxamide, N-[(2E)-3- (2,6,6-trimethyl-3-cyclohexen-1- yl)-2-butenyl]- 56

Cyclopropanecarboxamide, N-[(2Z)-3- (2,6,6-trimethyl-3-cyclohexen-1- yl)-2-butenyl]- 57

Cyclopropanecarboxamide, N-[(2E)-3- (2,4-dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 58

Cyclopropanecarboxamide, N-[(2Z)-3- (2,4-dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 59

Acetamide, N-[(2E)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]- 60

Acetamide, N-[(2Z)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]- 61

Acetamide, N-[(2E)-3-(2,6,6- trimethyl-3-cyclohexen-1-yl)-2- butenyl]- 62

Acetamide, N-[(2Z)-3-(2,6,6- trimethyl-3-cyclohexen-1-yl)-2- butenyl]- 63

Acetamide, N-[(2E)-3-(2,4-dimethyl- 3-cyclohexen-1-yl)-2-propenyl]- 64

Acetamide, N-[(2Z)-3-(2,4-dimethyl- 3-cyclohexen-1-yl)-2-propenyl]- 65

Cyclopropanecarboxamide, N-[[2- methyl-2-(4-methyl-3- pentenyl)cyclopropyl]methyl]- 66

Cyclopropanecarboxamide, N-[[2- [(3Z)-3- hexenyl]cyclopropyl]methyl]- 68

Propanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]- 70

Acetamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]- 71

Cyclopropanecarboxamide, N-methyl- N-[(2Z,6Z)-2,6-nonadienyl]- 72

Cyclopropanecarboxamide, N-ethyl-N- [(2Z,6Z)-2,6-nonadienyl]- 73

Cyclopropanecarboxamide, N- [(2Z,6Z)-2,6-nonadienyl]-N-propyl- 74

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2Z,6Z)-2,6- nonadienyl]- 75

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2Z,6Z)-2,6- nonadienyl]- 76

Cyclopropanecarboxamide, N-ethenyl- N-[(2Z,6Z)-2,6-nonadienyl]- 77

Cyclopropanecarboxamide, N- [(2Z,6Z)-2,6-nonadienyl]-N-(2- propenyl)- 78

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2Z,6Z)- 2,6-nonadienyl]- 79

Cyclopropanecarboxamide, N-butyl-N- [(2Z,6Z)-2,6-nonadienyl]- 80

Cyclopropanecarboxamide, N- [(2Z,6Z)-2,6-nonadienyl)-N-(2- methylpropyl) 81

Cyclopropanecarboxamide, N-methyl- N-[(2E,6Z)-2,6-nonadienyl]- 82

Cyclopropanecarboxamide, N-ethyl-N- [(2E,6Z)-2,6-nonadienyl]- 83

Cyclopropanecarboxamide, N- [(2E,6Z)-2,6-nonadienyl]-N-propyl- 84

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2E,6Z)-2,6- nonadienyl]- 85

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2E,6Z)-2,6- nonadienyl]- 86

Cyclopropanecarboxamide, N-ethenyl- N-[(2E,6Z)-2,6-nonadienyl]- 87

Cyclopropanecarboxamide, N- [(2E,6Z)-2,6-nonadienyl]-N-(2- propenyl)- 88

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2E,6Z)- 2,6-nonadienyl]- 89

Cyclopropanecarboxamide, N-butyl-N- [(2E,6Z)-2,6-nonadienyl]- 90

Cyclopropanecarboxamide, N- [(2E,6Z)-2,6-nonadienyl]-N-(2- methylpropyl)- 91

Cyclopropanecarboxamide, N-methyl- N-[(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]- 92

Cyclopropanecarboxamide, N-ethyl- N-[(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]- 93

Cyclopropanecarboxamide, N-[(2E)-3- (3-cyclohexen-1-yl)-2-propenyl]-N- propyl 94

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]- 95

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)- N-[(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]- 96

Cyclopropanecarboxamide, N-ethenyl- N-[(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]- 97

Cyclopropanecarboxamide, N-[(2E)-3- (3-cyclohexen-1-yl)-2-propenyl]-N- (2-propenyl)- 98

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]- 99

Cyclopropanecarboxamide, N-butyl-N- [(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]- 100

Cyclopropanecarboxamide, N-[(2E)-3- (3-cyclohexen-1-yl)-2-propenyl]-N- (2-methylpropyl)- 101

Cyclopropanecarboxamide, N-methyl- N-[(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]- 102

Cyclopropanecarboxamide, N-ethyl-N- [(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]- 103

Cyclopropanecarboxamide, N-[(2Z)-3- (3-cyclohexen-1-yl)-2-propenyl]-N- propyl- 104

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]- 105

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)- N-[(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]- 106

Cyclopropanecarboxamide, N-ethenyl- N-[(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]- 107

Cyclopropanecarboxamide, N-[(2Z)-3- (3-cyclohexen-1-yl)-2-propenyl]-N- (2-propenyl)- 108

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]- 109

Cyclopropanecarboxamide, N-butyl-N- [(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]- 110

Cyclopropanecarboxamide, N-[(2Z)-3- (3-cyclohexen-1-yl)-2-propenyl]-N- (2-methylpropyl)- 111

Cyclopropanecarboxamide, N-methyl- N-[(2E)-2-methyl-3-phenyl-2- propenyl]- 112

Cyclopropanecarboxamide, N-ethyl-N- [(2E)-2-methyl-3-phenyl-2- propenyl]- 113

Cyclopropanecarboxamide, N-[(2E)-2- methyl-3-phenyl-2-propenyl]-N- propyl 114

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2E)-2-methyl-3- phenyl-2-propenyl]- 115

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)- N-[(2E)-2-methyl-3-phenyl-2- propenyl]- 116

Cyclopropanecarboxamide, N-ethenyl- N-[(2E)-2-metkyl-3-phenyl-2- propenyl]- 117

Cyclopropanecarboxamide, N-[(2E)-2- methyl-3-phenyl-2-propenyl]-N-(2- propenyl)- 118

Cyclopropanecarboxamide, N-[(2E)-2- methyl-3-phenyl-2-propenyl]-N- (cyclopropylmethyl)- 119

Cyclopropanecarboxamide, N-butyl-N- [(2E)-2-methyl-3-phenyl-2- propenyl]- 120

Cyclopropanecarboxamide, N-[(2E)-2- methyl-3-phenyl-2-propenyl]-N-(2- methylpropyl)- 121

Cyclopropanecarboxamide, N-methyl- N-[(2Z)-2-methyl-3-phenyl-2- propenyl]- 122

Cyclopropanecarboxamide, N-ethyl-N- [(2Z)-2-methyl-3-phenyl-2- propenyl]- 123

Cyclopropanecarboxamide, N-[(2Z)-2- methyl-3-phenyl-2-propenyl]-N- propyl 124

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2Z)-2-methyl-3- phenyl-2-propenyl]- 125

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)- N-[(2Z)-2-methyl-3-phenyl-2- propenyl]- 126

Cyclopropanecarboxamide, N-ethenyl- N-[(2Z)-2--xnethyl-3-phenyl-2- propenyl]- 127

Cyclopropanecarboxamide, N-[(2Z)-2- methyl-3-phenyl-2-propenyl]-N-(2- propenyl)- 128

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2Z)-2- methyl-3-phenyl-2-propenyl]- 129

Cyclopropanecarboxamide, N-butyl- N-[(2Z)-2-methyl-3-phenyl-2- propenyl]- 130

Cyclopropanecarboxamide, N-[(2Z)-2- methyl-3-phenyl-2-propenyl)-N-(2- methylpropyl)- 131

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-butenyl]-N-methyl- 132

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-butenyl]-N-ethyl- 133

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-butenyl]-N-propyl- 134

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-butenyl)-N-(1- methylethyl)- 135

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-butenyl]-N-(1,1- dimethylethyl)- 136

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-butenyl]-N-ethenyl- 137

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-butenyl]-N-(2-propenyl)- 138

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-butenyl]-N- (cyclopropylmethyl)- 139

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-butenyl]-N-butyl- 140

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-butenyl]-N-(2- methylpropyl)- 141

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-butenyl]-N-methyl- 142

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-butenyl]-N-ethyl- 143

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-butenyl]-N-propyl- 144

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-butenyl]-N-(1- methylethyl)- 145

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-butenyl]-N-(1,1- dimethylethyl)- 146

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-butenyl]-N-ethenyl- 147

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-butenyl]-N-(2-propenyl)- 148

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-butenyl]-N- (cyclopropylmethyl)- 149

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-butenyl]-N-butyl- 150

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-butenyl]-N-(2- methylpropyl)- 151

Cyclopropanecarboxamide, N-methyl- N-[(2Z,6Z)-2-methyl-2,6- nonadienyl]- 152

Cyclopropanecarboxamide, N-ethyl-N- [(2Z,6Z)-2-methyl-2,6-nonadienyl]- 153

Cyclopropanecarboxamide, N- [(2Z,6Z)-2-methyl-2,6-nonadienyl]- N-propyl- 154

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2Z,6Z)-2-methyl- 2,6-nonadienyl]- 155

Cyclopropanecarboxamide, N-(2- methylpropyl)- N-[(2Z,6Z)-2-methyl-2,6- nonadienyl]- 156

Cyclopropanecarboxamide, N-ethenyl- N-[(2Z,6Z)-2-methyl-2,6- nonadienyl]- 157

Cyclopropanecarboxamide, N- [(2Z,6Z)-2-methyl-2,6-nonadienyl]- N-(2-propenyl)- 158

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2Z,6Z)-2- methyl-2,6-nonadienyl]- 159

Cyclopropanecarboxamide, N-butyl-N- [(2Z,6Z)-2-methyl-2,6-nonadienyl]- 160

Cyclopropanecarboxamide, N- [(2Z,6Z)-2-methyl-2,6-nonadienyl]- N-(2-methylpropyl)- 161

Cyclopropanecarboxamide, N-methyl- N-[(2E,6Z)-2-methyl-2,6- nonadienyl]- 162

Cyclopropanecarboxamide, N-ethyl-N- [(2E,6Z)-2-methyl-2,6-nonadienyl]- 163

Cyclopropanecarboxamide, N- [(2E,6Z)-2-methyl-2,6-nonadienyl]- N-propyl- 164

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2E,6Z)-2-methyl- 2,6-nonadienyl]- 165

Cyclopropanecarboxamide, N-(1,1- dimethylethyl]- N-[(2E,6Z)-2-methyl-2,6- nonadienyl]- 166

Cyclopropanecarboxamide, N-ethenyl- N-[(2E,6Z)-2-methyl-2,6-nonadienyl]- 167

Cyclopropanecarboxamide, N- [(2E,6Z)-2-methyl-2,6-nonadienyl]- N-(2-propenyl)- 168

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2E,6Z)-2- methyl-2,6-nonadienyl]- 169

Cyclopropanecarboxamide, N-butyl- N-[(2E,6Z)-2-methyl-2,6- nonadienyl]- 170

Cyclopropanecarboxamide, N- [(2E,6Z)-2-methyl-2,6-nonadienyl]- N-(2-methylpropyl)- 171

Cyclopropanecarboxamide, N-methyl- N-[(2E)-3-phenyl-2-propenyl]- 172

Cyclopropanecarboxamide, N-ethyl-N- [(2E)-3-phenyl-2-propenyl]- 173

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-propenyl]-N-propyl- 174

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2E)-3-phenyl-2- propenyl]- 175

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2E)-3-phenyl-2- propenyl]- 176

Cyclopropanecarboxamide, N-ethenyl- N-[(2E)-3-phenyl-2-propenyl]- 177

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-propenyl]-N-(2-propenyl)- 178

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2E)-3- phenyl-2-propenyl]- 179

Cyclopropanecarboxamide, N-butyl-N- [(2E)-3-phenyl-2-propenyl]- 180

Cyclopropanecarboxamide, N-[(2E)-3- phenyl-2-propenyl]-N-(2- methylpropyl)- 181

Cyclopropanecarboxamide, N-methyl- N-[(2Z)-3-phenyl-2-propenyl]- 182

Cyclopropanecarboxamide, N-ethyl-N- [(2Z)-3-phenyl-2-propenyl]- 183

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-propenyl]-N-propyl 184

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2Z)-3-phenyl-2- propenyl]- 185

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)- N-[(2Z)-3-phenyl-2- propenyl]- 186

Cyclopropanecarboxamide, N-ethenyl- N-[(2Z)-3-phenyl-2-propenyl]- 187

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-propenyl]-N-2-propenyl- 188

Cyclopropanecarboxamide, N- (cyclopropylrnethyl)-N-[(2Z)-3- phenyl-2-propenyl]- 189

Cyclopropanecarboxamide, N-butyl-N- [(2Z)-3-phenyl-2-propenyl]- 190

Cyclopropanecarboxamide, N-[(2Z)-3- phenyl-2-propenyl]-N-(2- methylpropyl)- 191

Propanamide, N-methyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-2,2- dimethyl- 192

Propanamide, N-ethyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-2,2- dimethyl- 193

Propanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-propyl-2,2- dimethyl- 194

Propanamide, N-(1-methylethyl)-N- [(2E)-3,7-dimethyl-2,6-octadienyl]- 2,2-dimethyl- 195

Propanamide, N-(1,1-dimethylethyl)- N-[(2E)-3,7-dimethyl-2,6- octadienyl]-2,2-dimethyl- 196

Propanamide, N-ethenyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-2,2- dimethyl- 197

Propanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-(2-propenyl)-2,2- dimethyl- 198

Propanamide, N-(cyclopropylmethyl)- N-[(2E)-3,7-dimethyl-2,6- octadienyl]-2,2-dimethyl- 199

Propanamide, N-butyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-2,2- dimethyl- 200

Propanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-(2-methylpropyl)- 2,2-dimethyl- 201

Propanamide, N-methyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-2,2- dimethyl- 202

Propanamide, N-ethyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-2,2- dimethyl- 203

Propanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-propyl-2,2- dimethyl- 204

Propanamide, N-(1-methylethyl)-N- [(2Z)-3,7-dimethyl-2,6-octadienyl]- 2,2-dimethyl- 205

Propanamide, N-(1,1-dimethylethyl)- N-[(2Z)-3,7-dimethyl-2,6- octadienyl]-2,2-dimethyl- 206

Propanamide, N-ethenyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-2,2- dimethyl- 207

Propanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-(2-propenyl)-2,2- dimethyl- 208

Propanamide, N-(cyclopropylmethyl)- N-[(2Z)-3,7-dimethyl-2,6- octadienyl]-2,2-dimethyl- 209

Propanamide, N-butyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-2,2- dimethyl- 210

Propanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl)-N-(2-methylpropyl)- 2,2-dimethyl- 211

Butanamide, N-methyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]- 212

Butanamide, N-ethyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]- 213

Butanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-propyl- 214

Butanamide, N-(1-methylethyl)-N- [(2E)-3,7-dimethyl-2,6-octadienyl]- 215

Butanamide, N-(1,1-dimethylethyl)- N-[(2E)-3,7-dimethyl-2,6- octadienyl]- 216

Butanamide, N-ethenyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]- 217

Butanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-(2-propenyl)- 218

Butanamide, N-(cyclopropylmethyl)- N-[(2E)-3,7-dimethyl-2,6- octadienyl]- 219

Butanamide, N-butyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]- 220

Butanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-(2-methylpropyl)- 221

Butanamide, N-methyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]- 222

Butanamide, N-ethyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]- 223

Butanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-propyl- 224

Butanamide, N-(1-methylethyl)-N- [(2Z)-3,7-dimethyl--2,6-octadienyl]- 225

Butanamide, N-(1,1-dimethylethyl)- N-[(2Z)-3,7-dimethyl-2,6- octadienyl]- 226

Butanamide, N-ethenyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]- 227

Butanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-(2-propenyl)- 228

Butanamide, N-(cyclopropylmethyl)- N-[(2Z)-3,7-dimethyl-2,6- octadienyl]- 229

Butanamide, N-butyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]- 230

Butanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-(2-methylpropyl)- 231

Propanamide, N-methyl-N-[(2E)-2- methyl-3-phenyl-2-propenyl]- 232

Propanamide, N-ethyl-N-[(2E)-2- methyl-3-phenyl-2-propenyl]- 233

Propanamide, N-[(2E)-2-methyl-3- phenyl-2-propenyl]-N-propyl- 234

Propanamide, N-(1-methylethyl)-N- [(2E)-2-methyl-3-phenyl-2- propenyl]- 235

Propanamide, N-(1,1-dimethylethyl)- N-[(2E)-2-methyl-3-phenyl-2- propenyl]- 236

Propanamide, N-ethenyl-N-[(2E)-2- methyl-3-phenyl-2-propenyl]- 237

Propanamide, N-[(2E)-2-methyl-3- phenyl-2-propenyl]-N-(2-propenyl)- 238

Propanamide, N-(cyclopropylmethyl)- N-[(2E)-2-methyl-3-phenyl-2- propenyl]- 239

Propanamide, N-butyl-N-[(2E)-2- methyl-3-phenyl-2-propenyl]- 240

Propanamide, N-[(2E)-2-methyl-3- phenyl-2-propenyl]-N-(2- methylpropyl)- 241

Propanamide, N-methyl-N-[(2Z)-2- methyl-3-phenyl-2-propenyl]- 242

Propanamide, N-ethyl-N-[(2Z)-2- methyl-3-phenyl-2-propenyl]- 243

Propanamide, N-[(2Z)-2-methyl-3- phenyl-2-propenyl]-N-propyl- 244

Propanamide, N-(1-methylethyl)-N- [(2Z)-2-methyl-3-phenyl-2- propenyl]- 245

Propanamide, N-(1-methylethyl)-N- [(2Z)-2-methyl-3-phenyl-2- propenyl]- 246

Propanamide, N-ethenyl-N-[(2Z)-2- methyl-3-phenyl-2-propenyl]- 247

Propanamide, N-[(2Z)-2-methyl-3- phenyl-2-propenyl]-N-2-propenyl- 248

Propanamide, N-(cyclopropylmethyl)- N-[(2Z)-2-methyl-3-phenyl-2- propenyl]- 249

Propanamide, N-butyl-N-[(2Z)-2- methyl-3-phenyl-2-propenyl]- 250

Propanamide, N-[(2Z)-2-methyl-3- phenyl-2-propenyl]-N-(2- methylpropyl)- 251

Propanamide, N-[(2E)-3-phenyl-2- butenyl]-N-methyl- 252

Propanamide, N-[(2E)-3-phenyl-2- butenyl]-N-ethyl- 253

Propanamide, N-[(2E)-3-phenyl-2- butenyl]-N-propyl- 254

Propanamide, N-[(2E)-3-phenyl-2- butenyl]-N-(1-methylethyl)- 255

Propanamide, N-[(2E)-3-phenyl-2- butenyl]-N-(1,1-dimethylethyl)- 256

Propanamide, N-[(2E)-3-phenyl-2- butenyl]-N-ethenyl- 257

Propanamide, N-[(2E)-3-phenyl-2- butenyl]-N-(2-propenyl)- 258

Propanamide, N-[(2E)-3-phenyl-2- butenyl]-N-(cyclopropylmethyl)- 259

Propanamide, N-[(2E)-3-phenyl-2- butenyl]-N-butyl- 260

Propanamide, N-[(2E)-3-phenyl-2- butenyl]-N-(2-methylpropyl)- 261

Propanamide, N-[(2Z)-3-phenyl-2- butenyl]-N-methyl- 262

Propanamide, N-[(2Z)-3-phenyl-2- butenyl]-N-ethyl- 263

Propanamide, N-[(2Z)-3-phenyl-2- butenyl]-N-propyl- 264

Propanamide, N-[(2Z)-3-phenyl-2- butenyl]-N-(1-methylethyl)- 265

Propanamide, N-[(2Z)- 3-phenyl-2- butenyl]-N-(1,1-dimethylethyl)- 266

Propanamide, N-[(2Z)-3-phenyl-2- butenyl]-N-ethenyl- 267

Propanamide, N-[(2Z)-3-phenyl-2- butenyl]-N-(2-propenyl)- 268

Propanamide, N-[(2Z)-3-phenyl-2- butenyl]-N-(cyclopropylmethyl)- 269

Propanamide, N-[(2Z)-3-phenyl-2- butenyl]-N-butyl- 270

Propanamide, N-[(2Z)-3-phenyl-2- butenyl]-N-(2-methylpropyl)- 271

Acetamide, N-methyl-N-[(2E)-2- methyl-3-phenyl-2-propenyl]- 272

Acetamide, N-ethyl-N-[(2E)-2- methyl-3-phenyl-2-propenyl]- 273

Acetamide, N-[(2E)-2-methyl-3- phenyl-2-propenyl]-N-propyl- 274

Acetamide, N-(1-methylethyl)-N- [(2E)-2-methyl-3-phenyl-2- propenyl]- 275

Acetamide, N-(1,1-dimethylethyl)-N- [(2E)-2-methyl-3-phenyl-2- propenyl]- 276

Acetamide, N-ethenyl-N-[(2E)-2- methyl-3-phenyl-2-propenyl]- 277

Acetamide, N-[(2E)-2-methyl-3- phenyl-2-propenyl]-N-(2-propenyl)- 278

Acetamide, N-(cyclopropylmethyl)-N- [(2E)-2-methyl-3-phenyl-2- propenyl]- 279

Acetamide, N-butyl-N-[(2E)-2- methyl-3-phenyl-2-propenyl]- 280

Acetamide, N-[(2E)-2-methyl-3- phenyl-2-propenyl]-N-(2- methylpropyl)- 281

Acetamide, N-methyl-N-[(2Z)-2- methyl-3-phenyl-2-propenyl]- 282

Acetamide, N-ethyl-N-[(2Z)-2- methyl-3-phenyl-2-propenyl]- 283

Acetamide, N-[(2Z)-2-methyl-3- phenyl-2-propenyl]-N-propyl- 284

Acetamide, N-(1-methylethyl)-N- [(2Z)-2-methyl-3-phenyl-2- propenyl]- 285

Acetamide, N-(1,1-dimethylethyl)-N- [(2Z)-2-methyl-3-phenyl-2- propenyl]- 286

Acetamide, N-ethenyl-N-[(2Z)-2- methyl-3-phenyl-2-propenyl]- 287

Acetamide, N-[(2Z)-2-methyl-3- phenyl-2-propenyl]-N-(2-propenyl)- 288

Acetamide, N-(cyclopropylmethyl)-N- [(2Z)-2-methyl-3-phenyl-2- propenyl]- 289

Acetamide, N-butyl-N-[(2Z)-2- methyl-3-phenyl-2-propenyl]- 290

Acetamide, N-[(2Z)-2-methyl-3- phenyl-2-propenyl]-N-(2- methylpropyl)- 291

Acetamide, N-[(2E)-3-phenyl-2- butenyl]-N-methyl- 292

Acetamide, N-[(2E)-3-phenyl-2- butenyl]-N-ethyl- 293

Acetamide, N-[(2E)-3-phenyl-2- butenyl]-N-propyl- 294

Acetamide, N-[(2E)-3-phenyl-2- butenyl]-N-(1-methylethyl)- 295

Acetamide, N-[(2E)-3-phenyl-2- butenyl]-N-(1,1-dimethylethyl)- 296

Acetamide, N-[(2E)-3-phenyl-2- butenyl]-N-ethenyl)- 297

Acetamide, N-[(2E)-3-phenyl-2- butenyl]-N-(2-propenyl)- 298

Acetamide, N-[(2E)-3-phenyl-2- butenyl]-N-(cyclopropylmethyl)- 299

Acetamide, N-[(2E)-3-phenyl-2- butenyl]-N-butyl- 300

Acetamide, N-[(2E)-3-phenyl-2- butenyl]-N-(2-methylpropyl)- 301

Acetamide, N-[(2Z)-3-phenyl-2- butenyl]-N-methyl- 302

Acetamide, N-[(2Z)-3-phenyl-2- butenyl]-N-ethyl- 303

Acetamide, N-[(2Z)-3-phenyl-2- butenyl]-N-propyl- 304

Acetamide, N-[(2Z)-3-phenyl-2- butenyl]-N-(1-methylethyl)- 305

Acetamide, N-[(2Z)-3-phenyl-2- butenyl]-N-(1,1-dimethylethyl)- 306

Acetamide, N-[(2Z)-3-phenyl-2- butenyl]-N-ethenyl)- 307

Acetamide, N-[(2Z)-3-phenyl-2- butenyl]-N-(2-propenyl)- 308

Acetamide, N-[(2Z)-3-phenyl-2- butenyl]-N-(cyclopropylmethyl)- 309

Acetamide, N-[(2Z)-3-phenyl-2- butenyl]-N-butyl- 310

Acetamide, N-[(2Z)-3-phenyl-2- butenyl]-N-(2-methylpropyl)- 311

Acetamide, N-methyl-N-[(2Z,6Z)-2- methyl-2,6-nonadienyl]- 312

Acetamide, N-ethyl-N-[(2Z,6Z)-2- methyl-2,6-nonadienyl]- 313

Acetamide, N-[(2Z,6Z)-2-methyl-2,6- nonadienyl]-N-propyl- 314

Acetamide, N-(1-methylethyl)-N- [(2Z,6Z)-2-methyl-2,6-nonadienyl]- 315

Acetamide, N-(1,1-dimethylethyl)-N- [(2Z,6Z)-2-methyl-2,6-nonadienyl]- 316

Acetamide, N-ethenyl-N-[(2Z,6Z)-2- methyl-2,6-nonadienyl]- 317

Acetamide, N-[(2Z,6Z)-2-methyl-2,6- nonadienyl]-N-(2-propenyl)- 318

Acetamide, N-(cyclopropylmethyl)-N- [(2Z,6Z)-2-methyl-2,6-nonadienyl]- 319

Acetamide, N-butyl-N-[(2Z,6Z)-2- methyl-2,6-nonadienyl]- 320

Acetamide, N-[(2Z,6Z)-2-methyl-2,6- nonadienyl]-N-(2-methylpropyl)- 321

Cyclopropylcarboxamide, N-methyl-N- [(2E,6Z)-2-methyl-2,6-nonadienyl]- 322

Cyclopropylcarboxamide, N-ethyl-N- [(2E,6Z)-2-methyl-2,6-nonadienyl]- 323

Cyclopropylcarboxamide, N-[(2E,6Z)- 2-methyl-2,6-nonadienyl]-N-propyl- 324

Cyclopropylcarboxamide, N-(1- methylethyl)-N-[(2E,6Z)-2-methyl- 2,6-nonadienyl]- 325

Cyclopropylcarboxamide, N-(1,1- dimethylethyl)-N-[(2E,6Z)-2-methyl- 2,6-nonadienyl]- 326

Cyclopropylcarboxamide, N-ethenyl- N-[(2E,6Z)-2-methyl-2,6- nonadienyl]- 327

Cyclopropylcarboxamide, N-[(2E,6Z)- 2-methyl-2,6-nonadienyl]-N-(2- propenyl)- 328

Cyclopropylcarboxamide, N- (cyclopropylmethyl)-N-[(2E,6Z)-2- methyl-2,6-nonadienyl]- 329

Cyclopropylcarboxamide, N-butyl-N- [(2E,6Z)-2-methyl-2,6-nonadienyl]- 330

Cyclopropylcarboxamide, N-[(2E,6Z)- 2-methyl-2,6-nonadienyl]-N-(2- methylpropyl)- 331

Propanamide, N-methyl-N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]- 332

Propanamide, N-ethyl-N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]- 333

Propanamide, N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]-N- propyl- 334

Propanamide, N-(1-methylethyl)-N- [(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]- 335

Propanamide, N-(1,1-dimethylethyl)- N-[(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]- 336

Propanamide, N-ethenyl-N-[(2E)-3- (3-cyclohexen-1-yl)-2-propenyl]- 337

Propanamide, N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]-N-(2- propenyl)- 338

Propanamide, N-(cyclopropylmethyl)- N-[(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]- 339

Propanamide, N-butyl-N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]- 340

Propanamide, N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]-N- (2-methylpropyl)- 341

Propanamide, N-methyl-N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]- 342

Propanamide, N-ethyl-N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]- 343

Propanamide, N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]-N- propyl- 344

Propanamide, N-(1-methylethyl)-N- [(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]- 345

Propanamide, N-(1,1-dimethylethyl)- N-[(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]- 346

Propanamide, N-ethenyl-N-[(2Z)-3- (3-cyclohexen-1-yl)-2-propenyl]- 347

Propanamide, N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]-N- (2-propenyl)- 348

Propanamide, N-(cyclopropylmethyl)- N-[(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]- 349

Propanamide, N-butyl-N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]- 350

Propanamide, N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]-N-(2- methylpropyl)- 351

Acetamide, N-methyl-N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]- 352

Acetamide, N-ethyl-N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]- 353

Acetamide, N-[(2E)-3-(3-cyclohexen- 1-yl)-2-propenyl]-N-propyl- 354

Acetamide, N-(1-methylethyl)-N- [(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]- 355

Acetamide, N-(1,1-dimethylethyl)-N- [(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]- 356

Acetamide, N-ethenyl-N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]- 357

Acetamide, N-[(2E)-3-(3-cyclohexen- 1-yl)-2-propenyl]-N-(2-propenyl)- 358

Acetamide, N-(cyclopropylmethyl)-N- [(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]- 359

Acetamide, N-butyl-N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]- 360

Acetamide, N-[(2E)-3-(3-cyclohexen- 1-yl)-2-propenyl)-N-(2- methylpropyl)- 361

Acetamide, N-methyl-N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]- 362

Acetamide, N-ethyl-N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]- 363

Acetamide, N-[(2Z)-3-(3-cyclohex 1-yl)-2-propenyl]-N-propyl- 364

Acetamide, N-(1-methylethyl)-N- [(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]- 365

Acetamide, N-(1,1-dimethylethyl) [(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]- 366

Acetamide, N-ethenyl-N-[(2Z)-3- (cyclohexen-1-yl)-2-propenyl]- 367

Acetamide, N-[(2Z)-3-(3-cyclohex 1-yl)-2-propenyl]-N-(2-propenyl) 368

Acetamide, N-(cyclopropylmethyl) [(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]- 369

Acetamide, N-butyl-N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]- 370

Acetamide, N-[(2Z)-3-(3-cyclohex 1-yl)-2-propenyl]-N-(2- methylpropyl]- 371

Propanamide, N-methyl-N-[(2E)-3- cyclohexen-1-yl)-2-propenyl]-2,2- dimethyl- 372

Propanamide, N-ethyl-N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]-2,2- dimethyl- 373

Propanamide, N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]-N- propyl-2,2-dimethyl- 374

Propanamide, N-(1-methylethyl)-N- [(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]-2,2-dimethyl- 375

Propanamide, N-(1,1-dimethylethyl)- N-[(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]-2,2-dimethyl- 376

Propanamide, N-ethenyl-N-[(2E)-3- (3-cyclohexen-1-yl)-2-propenyl]- 2,2-dimethyl- 377

Propanamide, N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]-N-(2- propenyl)-2,2-dimethyl- 378

Propanamide, N-(cyclopropylmethyl)- N-[(2E)-3-(3-cyclohexen-1-yl)-2- propenyl]-2,2-dimethyl- 379

Propanamide, N-butyl-N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]-2,2- dimethyl- 380

Propanamide, N-[(2E)-3-(3- cyclohexen-1-yl)-2-propenyl]-N-(2- methylpropyl)-2,2-dimethyl- 381

Propanamide, N-methyl-N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]-2,2- dimethyl- 382

Propanamide, N-ethyl-N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]-2,2- dimethyl- 383

Propanamide, N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]-N- propyl-2,2-dimethyl- 384

Propanamide, N-(1-methylethyl)-N- [(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]-2,2-dimethyl- 385

Propanamide, N-(1,1-dimethylethyl)- N-[(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]-2,2-dimethyl- 386

Propanamide, N-ethenyl-N-[(2Z)-3- (3-cyclohexen-1-yl)-2-propenyl]- 2,2-dimethyl- 387

Propanamide, N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]-N- (2-propenyl)-2,2-dimethyl- 388

Propanamide, N-(cyclopropylmethyl)- N-[(2Z)-3-(3-cyclohexen-1-yl)-2- propenyl]-2,2-dimethyl- 389

Propanamide, N-butyl-N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]-2,2- dimethyl- 390

Propanamide, N-[(2Z)-3-(3- cyclohexen-1-yl)-2-propenyl]-N-(2- methylpropyl)-2,2-dimethyl- 391

Butanamide, N-methyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 392

Butanamide, N-ethyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 393

Butanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-propyl-2-methyl- 394

Butanamide, N-(1-methylethyl)-N- [(2E)-3,7-dimethyl-2,6-octadienyl]- 2-methyl- 395

Butanamide, N-(1,1-dimethylethyl)- N-[(2E)-3,7-dimethyl-2,6- octadienyl]-2-methyl- 396

Butanamide, N-ethenyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 397

Butanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-(2-propenyl)-2- methyl- 398

Butanamide, N-(cyclopropylmethyl)- N-[(2E)-3,7-dimethyl-2,6- octadienyl]-2-methyl- 399

Butanamide, N-butyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 400

Butanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-(2-methylpropyl)- 2-methyl- 401

Butanamide, N-methyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 402

Butanamide, N-ethyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 403

Butanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-propyl-2-methyl- 404

Butanamide, N-(1-methylethyl)-N- [(2Z)-3,7-dimethyl-2,6-octadienyl]- 2-methyl- 405

Butanamide, N-(1,1-dimethylethyl)- N-[(2Z)-3,7-dimethyl-2,6- octadienyl]-2-methyl- 406

Butanamide, N-ethenyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 407

Butanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-(2-propenyl)-2- methyl- 408

Butanamide, N-(cyclopropylmethyl)- N-[(2Z)-3,7-dimethyl-2,6- octadienyl]-2-methyl- 409

Butanamide, N-butyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 410

Butanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl)-N-(2-methylpropyl)- 2-methyl- 411

Cyclopropanecarboxamide, N-methyl- N-[(2E)-3,7-dimethyl-2,6- octadienyl]- 412

Cyclopropanecarboxamide, N-ethyl-N- [(2E)-3,7-dimethyl-2,6-octadienyl]- 413

Cyclopropanecarboxamide, N-[(2E)- 3,7-dimethyl-2,6-octadienyl]-N- propyl- 414

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2E)-3,7-dimethyl- 2,6-octadienyl]- 415

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2E)-3,7- dimethyl-2,6-octadienyl]- 416

Cyclopropanecarboxamide, N-ethenyl- N-[(2E)-3,7-dimethyl-2,6- octadienyl]- 417

Cyclopropanecarboxamide, N-[(2E)- 3,7-dimethyl-2,6-octadienyl]-N- 2-propenyl- 418

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2E)-3,7- dimethyl-2,6-octadienyl]- 419

Cyclopropanecarboxamicie, N-butyl-N- [(2E)-3,7-dimethyl-2,6-octadienyl]- 420

Cyclopropanecarboxamide, N-[(2E)- 3,7-dimethyl-2,6-octadienyl]-N-(2- methylpropyl)- 421

Cyclopropanecarboxamide, N-methyl- N-[(2Z)-3,7-dimethyl-2,6- octadienyl]- 422

Cyclopropanecarboxamide, N-ethyl-N- [(2Z)-3,7-dimethyl-2,6-octadienyl]- 423

Cyclopropanecarboxamide, N-[(2Z)- 3,7-dimethyl-2,6-octadienyl)-N- propyl- 424

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]- 425

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]- 426

Cyclopropanecarboxamide, N-ethenyl- N-[(2Z)-3,7-dimethyl-2,6- octadienyl]- 427

Cyclopropanecarboxamide, N-[(2Z)- 3,7-dimethyl-2,6-octadienyl]-N-2- propenyl- 428

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]- 429

Cyclopropanecarboxamide, N-butyl-N- [(2Z)-3,7-dimethyl-2,6-octadienyl]- 430

Cyclopropanecarboxamide, N-[(2Z)- 3,7-dimethyl-2,6-octadienyl]-N-(2- methylpropyl)- 431

Propanamide, N-methyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 432

Propanamide, N-ethyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 433

Propanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-propyl-2-methyl- 434

Propanamide, N-(1-methylethyl)-N- [(2E)-3,7-dimethyl-2,6-octadienyl]- 2-methyl- 435

Propanamide, N-(1,1-dimethylethyl)- N-[(2E)-3,7-dimethyl-2,6- octadienyl]-2-methyl- 436

Propanamide, N-ethenyl-N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-2-methyl- 437

Propanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-(2-propenyl)-2- methyl- 438

Propanamide, N-(cyclopropylmethyl)- N-[(2E)-3,7-dimethyl-2,6- octadienyl]-2-methyl- 439

Propanamide, N-butyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 440

Propanamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-(2-methylpropyl)- 2-methyl- 441

Propanamide, N-methyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 442

Propanamide, N-ethyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 443

Propanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-propyl-2-methyl- 444

Propanamide, N-(1-methylethyl)-N- [(2Z)-3,7-dimethyl-2,6-octadienyl]- 2-methyl- 445

Propanamide, N-(1,1-dimethylethyl)- N-[(2Z)-3,7-dimethyl-2,6- octadienyl]-2-methyl- 446

Propanamide, N-ethenyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-2-methyl- 447

Propanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-(2-propenyl)-2- methyl- 448

Propanamide, N-(cyclopropylmethyl)- N-[(2Z)-3,7-dimethyl-2,6- octadienyl]-2-methyl- 449

Propanamide, N-butyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl)-2-methyl- 450

Propanamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-(2-methylpropyl)- 2-methyl- 451

2-butenamide, N-methyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-, (2E)- 452

2-butenamide, N-ethyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-, (2E)- 453

2-butenamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl)-N-propyl-, (2E)- 454

2-butenamide, N-(1-methylethyl)-N- [(2E)-3,7-dimethyl-2,6-octadienyl]-, (2E)- 455

2-butenamide, N-(1,1- dimethylethyl)-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-, (2E)- 456

2-butenamide, N-ethenyl-N-[(2E)- 3,7-dimethyl-2,6-octadienyl]-, (2E)- 457

2-butenamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-(2-propenyl)-, (2E)- 458

2-butenamide, N- (cyclopropylmethyl)-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-, (2E)- 459

2-butenamide, N-butyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-, (2E)- 460

2-butenamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-(2-methylpropyl)-, (2E)- 461

2-butenamide, N-methyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-, (2E)- 462

2-butenamide, N-ethyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-, (2E)- 463

2-butenamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-propyl-, (2E)- 464

2-butenamide, N-(1-methylethyl)-N- [(2Z)-3,7-dimethyl-2,6-octadienyl]-, (2E)- 465

2-butenamide, N-(1,1- dimethylethyl)-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-, (2E)- 466

2-butenamide, N-ethenyl-N-[(2Z)- 3,7-dimethyl-2,6-octadienyl]-, (2E)- 467

2-butenamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-(2-propenyl)-, (2E)- 468

2-butenamide, N- (cyclopropylmethyl)-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-, (2E)- 469

2-butenamide, N-butyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-, (2E)- 470

2-butenamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-(2-methylpropyl)-, (2E)- 471

2-butenamide, N-methyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-3-methyl- 472

2-butenamide, N-ethyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-3-methyl- 473

2-butenamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-propyl-3-methyl- 474

2-butenamide, N-(1-methylethyl)-N- [(2E)-3,7-dimethyl-2,6-octadienyl]- 3-methyl- 475

2-butenamide, N-(1,1- dimethylethyl)-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-3-methyl- 476

2-butenamide, N-ethenyl-N-[(2E)- 3,7-dimethyl-2,6-octadienyl]-3- mehtyl- 477

2-butenamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-(2-propenyl)-3- methyl- 478

2-butenamide, N- (cyclopropylmethyl)-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-3-methyl- 479

2-butenamide, N-butyl-N-[(2E)-3,7- dimethyl-2,6-octadienyl]-3-methyl- 480

2-butenamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-N-(2-methylpropyl)- 3-methyl- 481

2-butenamide, N-methyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-3-methyl- 482

2-butenamide, N-ethyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-3-methyl- 483

2-butenamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-propyl-3-methyl- 484

2-butenamide, N-(1-methylethyl)-N- [(2Z)-3,7-dimethyl-2,6-octadienyl]- 3-methyl- 485

2-butenamide, N-(1,1- dimethylethyl)-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-3-methyl- 486

2-butenamide, N-ethenyl-N-[(2Z)- 3,7-dimethyl-2,6-octadienyl]-3- methyl- 487

2-butenamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-(2-propenyl)-3- methyl- 488

2-butenamide, N- (cyclopropylmethyl)-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-3-methyl- 489

2-butenamide, N-butyl-N-[(2Z)-3,7- dimethyl-2,6-octadienyl]-3-methyl- 490

2-butenamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-N-(2-methylpropyl)- 3-methyl- 491

Cyclopropanecarboxamide, N- [(2E,6Z)-2,6-dodecadienyl]-N- methyl- 492

Cyclopropanecarboxamide, N- [(2E,6Z)-2,6-dodecadienyl]-N-ethyl- 493

Cyclopropanecarboxamide, N- [(2E,6Z)-2,6-dodecadienyl]-N- propyl- 494

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2E,6Z)-2,6- dodecadienyl]- 495

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2E,6Z)-2,6- dodecadienyl]- 496

Cyclopropanecarboxamide, N-ethenyl- N-[(2E,6Z)-2,6-dodecadienyl]- 497

Cyclopropanecarboxamide, N- [(2E,6Z)-2,6-dodecadienyl]-N-(2- propenyl)- 498

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2E,6Z)-2,6- dodecadienyl]- 499

Cyclopropanecarboxamide, N-butyl-N- [(2E,6Z)-2,6-dodecadienyl]- 500

Cyclopropanecarboxamide, N- [(2E,6Z)-2,6-dodecadienyl]-N-(2- methylpropyl)- 501

Cyclopropanecarboxamide, N- [(2Z,6Z)-2,6-dodecadienyl]-N- methyl- 502

Cyclopropanecarboxamide, N- [(2Z,6Z)-2,6-dodecadienyl]-N-ethyl- 503

Cyclopropanecarboxamide, N- [(2Z,6Z)-2,6-dodecadienyl]-N- propyl- 504

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2Z,6Z)-2,6- dodecadienyl]- 505

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2Z,6Z)-2,6- dodecadienyl]- 506

Cyclopropanecarboxamide, N-ethenyl- N-[(2Z,6Z)-2,6-dodecadienyl]- 507

Cyclopropanecarboxamide, N- [(2Z,6Z)-2,6-dodecadienyl]-N-(2- propenyl)- 508

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2Z,6Z)-2,6- dodecadienyl]- 509

Cyclopropanecarboxamide, N-butyl-N- [(2Z,6Z)-2,6-dodecadienyl]- 510

Cyclopropanecarboxamide, N- [(2Z,6Z)-2,6-dodecadienyl]-N-(2- methylpropyl)- 511

Cyclopropanecarboxamide, N-[(2E)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-methyl- 512

Cyclopropanecarboxamide, N-[(2E)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-ethyl- 513

Cyclopropanecarboxamide, N-[(2E)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-propyl- 514

Cyclopropanecarboxamide, N-[(2E)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-(1-methylethyl)- 515

Cyclopropanecarboxamide, N-[(2E)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-(1,1-dimethylethyl)- 516

Cyclopropanecarboxamide, N-[(2E)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-ethenyl- 517

Cyclopropanecarboxamide, N-[(2E)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-(2-propenyl)- 518

Cyclopropanecarboxamide, N-[(2E)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-(cyclopropylmethyl)- 519

Cyclopropanecarboxamide, N-[(2E)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-butyl- 520

Cyclopropanecarboxamide, N-[(2E)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-(2-methylpropyl)- 521

Cyclopropanecarboxamide, N-[(2Z)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-methyl- 522

Cyclopropanecarboxamide, N-[(2Z)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-ethyl- 523

Cyclopropanecarboxamide, N-[(2Z)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-propyl- 524

Cyclopropanecarboxamide, N-[(2Z)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-(1-methylethyl)- 525

Cyclopropanecarboxamide, N-[(2Z)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-(1,1-dimethylethyl)- 526

Cyclopropanecarboxamide, N-[(2Z)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-ethenyl- 527

Cyclopropanecarboxamide, N-[(2Z)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-(2-propenyl)- 528

Cyclopropanecarboxamide, N-[(2Z)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-(cyclopropylmethyl)- 529

Cyclopropanecarboxamide, N-[(2Z)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-butyl- 530

Cyclopropanecarboxamide, N-[(2Z)-3- (4-methyl-3-cyclohexen-1-yl)-2- butenyl]-N-(2-methylpropyl)- 531

Cyclopropanecarboxamide, N-(3- methyl-2-butenyl)-N-methyl- 532

Cyclopropanecarboxamide, N-(3- methyl-2-butenyl)-N-ethyl- 533

Cyclopropanecarboxamide, N-(3- methyl-2-butenyl)-N-propyl- 534

Cyclopropanecarboxamide, N-(3- methyl-2-butenyl)-N-(1- methylethyl)- 535

Cyclopropanecarboxamide, N-(3- methyl-2-butenyl)-N-(1,1- dimethylethyl)- 536

Cyclopropanecarboxamide, N-(3- methyl-2-butenyl)-N-ethenyl- 537

Cyclopropanecarboxamide, N-(3- methyl-2-butenyl)-N-(2-propenyl)- 538

Cyclopropanecarboxamide, N-(3- methyl-2-butenyl)-N- (cyclopropylmethyl)- 539

Cyclopropanecarboxamide, N-(3- methyl-2-butenyl)-N-butyl- 540

Cyclopropanecarboxamide, N-(3- methyl-2-butenyl)-N-(2- methylpropyl)- 541

Cyclopropanecarboxamide, N-methyl- N-[(2E)-3-(2,4-dimethyl-3- cyclohexen-1-yl)-2-propenyl]- 542

Cyclopropanecarboxamide, N-ethyl-N- [(2E)-3-(2,4-dimethyl-3-cyclohexen- 1-yl)-2-propenyl]- 543

Cyclopropanecarboxamide, N-[(2E)-3- (2,4-dimethyl-3-cyclohexen-1-yl)-2- propenyl]-N-propyl- 544

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2E)-3-(2,4- dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 545

Cyclopropanecarboxamide, N-(1,1- methylethyl)-N-[(2E)-3-(2,4- dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 546

Cyclopropanecarboxamide, N-ethenyl- N-[(2E)-3-(2,4-dixnethyl-3- cyclohexen-1-yl)-2-propenyl]- 5547

Cyclopropanecarboxamide, N-[(2E)-3- (2,4-dimethyl-3-cyclohexen-1-yl)-2- propenyl]-N-(2-propenyl)- 548

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-[(2E)-3-(2,4- dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 549

Cyclopropanecarboxamide, N-butyl-N- [(2E)-3-(2,4-dimethyl-3-cyclohexen- 1-yl)-2-propenyl]- 550

Cyclopropanecarboxamide, N-[(2E)-3- (2,4-dimethyl-3-cyclohexen-1-yl)-2- propenyl]-N-(2-methylpropyl)- 551

Cyclopropanecarboxamide, N-methyl- N-[(2Z)-3-(2,4-dimethyl-3- cyclohexen-1-yl)-2-propenyl]- 552

Cyclopropanecarboxamide, N-ethyl-N- [(2Z)-3-(2,4-dimethyl-3-cyclohexen- 1-yl)-2-propenyl]- 553

Cyclopropanecarboxamide, N-[(2Z)-3- (2,4-dimethyl-3-cyclohexen-1-yl)-2- propenyl]-N-propyl- 554

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2Z)-3-(2,4- dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 555

Cyclopropanecarboxamide, N-(1,1- methylethyl)-N-[(2Z)-3-(2,4- dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 556

Cyclopropanecarboxamide, N-ethenyl- N-[(2Z)-3-(2,4-dimethyl-3- cyclohexen-1-yl)-2-propenyl]- 557

Cyclopropanecarboxamide, N-[(2Z)-3- (2,4-dimethyl-3-cyclohexen-1-yl)-2- propenyl]-N-(2-propenyl)- 558

Cyclopropanecarboxamide, N- (cyclopropylmethyl)-N-∂(2Z)-3-(2,4- dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 559

Cyclopropanecarboxamide, N-butyl-N- [(2Z)-3-(2,4-dimethyl-3-cyclohexen- 1-yl)-2-propenyl]- 560

Cyclopropanecarboxamide, N-[(2Z)-3- (2,4-dimethyl-3-cyclohexen-1-yl)-2- propenyl]-N-(2-methylpropyl)- 561

Acetamide, N-[(2E)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N- methyl- 562

Acetamide, N-[(2E)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N- ethyl- 563

Acetamide, N-[(2E)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N- propyl- 564

Acetamide, N-[(2E)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N-(1- methylethyl]- 565

Acetamide, N-[(2E)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N-(1,1- dimethylethyl]- 566

Acetamide, N-[(2E)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N- ethenyl- 567

Acetamide, N-[(2E)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N-(2- propenyl)- 568

Acetamide, N-[(2E)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N- (cyclopropylmethyl)- 569

Acetamide, N-[(2E)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N- butyl- 570

Acetamide, N-[(2E)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N-(2- methylpropyl)- 571

Acetamide, N-[(2Z)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N- methyl- 572

Acetamide, N-[(2Z)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N- ethyl- 573

Acetamide, N-[(2Z)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N- propyl- 574

Acetamide, N-[(2Z)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N-(1- methylethyl)- 575

Acetamide, N-[(2Z)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N-(1,1- dimethylethyl)- 576

Acetamide, N-[(2Z)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl)-N- ethenyl- 577

Acetamide, N-[(2Z)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N-(2- propenyl)- 578

Acetamide, N-[(2Z)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N- (cyclopropylmethyl)- 579

Acetamide, N-[(2Z)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N- butyl- 580

Acetamide, N-[(2Z)-3-(4-methyl-3- cyclohexen-1-yl)-2-butenyl]-N-(2- methylpropyl)- 581

Acetamide, N-methyl-N-[(2E)-3-(2,4- dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 582

Acetamide, N-ethyl-N-[(2E)-3-(2,4- dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 583

Acetamide, N-[(2E)-3-(2,4-dimethyl- 3-cyclohexen-1-yl)-2-propenyl]-N- propyl- 584

Acetamide, N-(1-methylethyl)-N- [(2E)-3-(2,4-dimethyl-3-cyclohexen- 1-yl)-2-propenyl]- 585

Acetamide, N-(1,1-dimethylethyl)-N- [(2E)-3-(2,4-dimethyl-3-cyclohexen- 1-yl)-2-propenyl]- 586

Acetamide, N-ethenyl-N-[(2E)-3- (2,4-dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 587

Acetamide, N-[(2E)-3-(2,4-dimethyl- 3-cyclohexen-1-yl)-2-propenyl]-N- (2-propenyl)- 588

Acetamide, N-(cyclopropylmethyl)-N- [(2E)-3-(2,4-dimethyl-3-cyclohexen- 1-yl)-2-propenyl]- 589

Acetamide, N-butyl-N-[(2E)-3-(2,4- dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 590

Acetamide, N-[(2E)-3-(2,4-dimethyl- 3-cyclohexen-1-yl)-2-propenyl)-N- (2-methylpropyl)- 591

Acetamide, N-methyl-N-[(2Z)-3-(2,4- dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 592

Acetamide, N-ethyl-N-[(2Z)-3-(2,4- dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 593

Acetamide, N-[(2Z)-3-(2,4-dimethyl- 3-cyclohexen-1-yl)-2-propenyl]-N- propyl- 594

Acetamide, N-(1-methylethyl)-N- [(2Z)-3-(2,4-dimethyl-3-cyclohexen- 1-yl)-2-propenyl]- 595

Acetamide, N-(1,1-dimethylethyl)-N- [(2Z)-3-(2,4-dimethyl-3-cyclohexen- 1-yl)-2-propenyl]- 596

Acetamide, N-ethenyl-N-[(2Z)-3- (2,4-dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 597

Acetamide, N-[(2Z)-3-(2,4-dimethyl- 3-cyclohexen-1-yl)-2-propenyl]-N- (2-propenyl)- 598

Acetamide, N-(cyclopropylmethyl)-N- [(2Z)-3-(2,4-dimethyl-3-cyclohexen- 1-yl)-2-propenyl]- 599

Acetamide, N-butyl-N-[(2Z)-3-(2,4- dimethyl-3-cyclohexen-1-yl)-2- propenyl]- 600

Acetamide, N-[(2Z)-3-(2,4-dimethyl- 3-cyclohexen-1-yl)-2-propenyl]-N- (2-methylpropyl)- 601

Propanamide, N-methyl-N-(2,6- nonadienyl)- 602

Propanamide, N-ethyl-N-(2,6- nonadienyl)- 603

Propanamide, N-(2,6-nonadienyl)-N- propyl- 604

Propanamide, N-(1-methylethyl)-N- (2,6-nonadienyl)- 605

Propanamide, N-(1,1-dimethylethyl)- N-(2,6-nonadienyl)- 606

Propanamide, N-ethenyl-N-(2,6- nonadienyl)- 607

Propanamide, N-(2,6-nonadienyl)-N- (2-propenyl)- 608

Propanamide, N-(cyclopropylmethyl)- N-(2,6-nonadienyl)- 609

Propanamide, N-butyl-N-(2,6- nonadienyl)- 610

Propanamide, N-(2,6-nonadienyl)-N- (2-methylpropyl)- 611

Propanamide, N-methyl-N-(2,6- nonadienyl)- 612

Propanamide, N-ethyl-N-(2,6- nonadienyl)- 613

Propanamide, N-(2,6-nonadienyl)-N- propyl- 614

Propanamide, N-(1-methylethyl)-N- (2,6-nonadienyl)- 615

Propanamide, N-(1,1-dimethylethyl)- N-(2,6-nonadienyl)-

Compound # Structure (Novel compounds) CA Index Name 616

Propanamide, N-ethenyl-N-(2,6- nonadienyl)- 617

Propanamide, N-(2,6-nonadienyl)-N- (2-propenyl)- 618

Propanamide, N-(cyclopropylmethyl)- N-(2,6-nonadienyl)- 619

Propanamide, N-butyl-N-(2,6- nonadienyl)- 620

Propanamide, N-(2,6-nonadienyl)-N- (2-methylpropyl)- 621

Acetamide, N-methyl-N-(2,6- nonadienyl)- 622

Acetamide, N-ethyl-N-(2,6- nonadienyl)- 623

Acetamide, N-(2,6-nonadienyl)-N- propyl- 624

Acetamide, N-(1-methylethyl)-N- (2,6-nonadienyl)- 625

Acetamide, N-(1,1-dimethylethyl)-N- (2,6-nonadienyl)- 626

Acetamide, N-ethenyl-N-(2,6- nonadienyl)- 627

Acetamide, N-(2,6-nonadienyl)-N-(2- propenyl)- 628

Acetamide, N-(cyclopropylmethyl)-N- (2,6-nonadienyl)- 629

Acetamide, N-butyl-N-(2,6- nonadienyl)- 630

Acetamide, N-(2,6-nonadienyl)-N-(2- methylpropyl)- 631

Acetamide, N-methyl-N-(2,6- nonadienyl)- 632

Acetamide, N-ethyl-N-(2,6- nonadienyl)- 633

Acetamide, N-(2,6-nonadienyl)-N- propyl- 634

Acetamide, N-(1-methylethyl)-N- (2,6-nonadienyl)- 635

Acetamide, N-(1,1-dimethylethyl)-N- (2,6-nonadienyl)- 636

Acetamide, N-ethenyl-N-(2,6- nonadienyl)- 637

Acetamide, N-(2,6-nonadienyl)-N-(2- propenyl)- 638

Acetamide, N-(cyclopropylmethyl)-N- (2,6-nonadienyl)- 639

Acetamide, N-butyl-N-(2,6- nonadienyl)- 640

Acetamide, N-(2,6-nonadienyl)-N-(2- methylpropyl)- 641

Cyclopropanecarboxamide, N-[[2- [(3Z)-3- hexenyl]cyclopropyl]methyl]-N- methyl- 642

Cyclopropanecarboxamide, N-ethyl-N- [[2-[(3Z)-3- hexenyl]cyclopropyl]methyl]- 643

Cyclopropanecarboxamide, N-[[2- [(3Z)-3- hexenyl]cyclopropyl]methyl]-N- propyl- 644

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-[(3Z)-3- hexenyl]cyclopropyl]methyl]- 645

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[[2-[(3Z)-3- hexenyl]cyclopropyl]methyl]- 646

Cyclopropanecarboxamide, N-ethenyl- N-[[2-[(3Z)-3- hexenyl]cyclopropyl]methyl]- 647

Cyclopropanecarboxamide, N-[[2- [(3Z)-3- hexenyl]cyclopropyl]methyl]-N-(2- propenyl)- 648

Cyclopropanecarboxamide, N-[[2- [(3Z)-3- hexenyl]cyclopropyl]methyl]-N- (cyclopropylmethyl)- 649

Cyclopropanecarboxamide, N-butyl-N- [[2-[(3Z)-3- hexenyl]cyclopropyl]methyl]- 650

Cyclopropanecarboxamide, N-[[2- [(3Z)-3- hexenyl]cyclopropyllmethyl]-N-(2- methylpropyl)- 651

Cyclopropanecarboxamide, N-[[2- [(3Z)-3- hexenyl]cyclopropyl]methyl)-N- methyl- 652

Cyclopropanecarboxamide, N-ethyl-N- [[2-[(3Z)-3- hexenyl]cyclopropyl]methyl]- 653

Cyclopropanecarboxamide, N-[[2- [(3Z)-3- hexenyl]cyclopropyl]methyl]-N- propyl- 654

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[[2-[(3Z)-3- hexenyl]cyclopropyl]methyl]- 655

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[[2-[(3Z)-3- hexenyl]cyclopropyl]methyl]- 656

Cyclopropanecarboxamide, N-ethenyl- N-[[2-[(3Z)-3- hexenyl]cyclopropyl]methyl]- 657

Cyclopropanecarboxamide, N-[[2- [(3Z)-3- hexenyl]cyclopropyl]methyl]-N-(2- propenyl)- 658

Cyclopropanecarboxamide, N-[[2- [(3Z)-3- hexenyl]cyclopropyl]methyl]-N- (cyclopropylmethyl)- 659

Cyclopropanecarboxamide, N-butyl-N- [[2-[(3Z)-3- hexenyl]cyclopropylimethyl]- 660

Cyclopropanecarboxamide, N-[[2- [(3Z)-3- hexenyl]cyclopropyl]methyl]-N-(2- methylpropyl)- 661

Cyclopropanecarboxamide, N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-methyl- 662

Cyclopropanecarboxamide, N-ethyl-N- [(2-[3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 663

Cyclopropanecarboxamide, N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-propyl- 664

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-[3-cyclohexen- 1-yl]-cyclopropyl)-methyl]- 665

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 666

Cyclopropanecarboxamide, N-ethenyl- N-[(2-[3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 667

Cyclopropanecarboxamide, N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-(2-propenyl)- 668

Cyclopropanecarboxamide, N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)- 669

Cyclopropanecarboxamide, N-butyl-N- [(2-[3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 670

Cyclopropanecarboxamide, N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-(2-methylpropyl)- 671

Cyclopropanecarboxamide, N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-methyl- 672

Cyclopropanecarboxamide, N-ethyl-N- [(2-[3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 673

Cyclopropanecarboxamide, N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-propyl- 674

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-[3-cyclohexen-1- yl]-cyclopropyl)-methyl)- 675

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-[3-cyclohexen- 1-yl]-cyclopropyl)-methyl]- 676

Cyclopropanecarboxamide, N-ethenyl- N-[(2-[3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 677

Cyclopropanecarboxamide, N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-(2-propenyl)- 678

Cyclopropanecarboxamide, N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)- 679

Cyclopropanecarboxamide, N-butyl-N- [(2-[3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 680

Cyclopropanecarboxamide, N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-(2-methylpropyl)- 681

Cyclopropanecarboxamide, N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]-N-methyl- 682

Cyclopropanecarboxamide, N-ethyl-N- [(1-methyl-2-phenyl-cyclopropyl)- methyl]- 683

Cyclopropanecarboxamide, N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]-N-propyl- 684

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]- 685

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(1-methyl-2- phenyl-cyclopropyl)-methyl]- 686

Cyclopropanecarboxamide, N-ethenyl- N-[(1-methyl-2-phenyl-cyclopropyl)- methyl]- 687

Cyclopropanecarboxamide, N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]-N-(2-propenyl)- 688

Cyclopropanecarboxamide, N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]-N-(cyclopropylmethyl)- 689

Cyclopropanecarboxamide, N-butyl-N- [(1-methyl-2-phenyl-cyclopropyl)- methyl]- 690

Cyclopropanecarboxamide, N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]-N-(2-methylpropyl)- 691

Cyclopropanecarboxamide, N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]-N-methyl- 692

Cyclopropanecarboxamide, N-ethyl-N- [(1-methyl-2-phenyl-cyclopropyl)- methyl]- 693

Cyclopropanecarboxamide, N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]-N-propyl- 694

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]- 695

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(1-methyl-2- phenyl-cyclopropyl)-methyl]- 696

Cyclopropanecarboxamide, N-ethenyl- N-[(1-methyl-2-phenyl-cyclopropyl)- methyl]- 697

Cyclopropanecarboxamide, N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]-N-(2-propenyl)- 698

Cyclopropanecarboxamide, N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]-N-(cyclopropylmethyl)- 699

Cyclopropanecarboxamide, N-butyl-N- [(1-methyl-2-phenyl-cyclopropyl)- methyl]- 700

Cyclopropanecarboxamide, N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]-N-(2-methylpropyl)- 701

Cyclopropanecarboxamide, N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]-N-methyl- 702

Cyclopropanecarboxamide, N-ethyl-N- [(2-methyl-2-phenyl-cyclopropyl)- methyl]- 703

Cyclopropanecarboxamide, N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]-N-propyl- 704

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]- 705

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-methyl-2- phenyl-cyclopropyl)-methyl]- 706

Cyclopropanecarboxamide, N-ethenyl- N-[(2-methyl-2-phenyl-cyclopropyl)- methyl]- 707

Cyclopropanecarboxamide, N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]-N-(2-propenyl)- 708

Cyclopropanecarboxamide, N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]-N-(cyclopropylmethyl)- 709

Cyclopropanecarboxamide, N-butyl-N- [(2-methyl-2-phenyl-cyclopropyl)- methyl]- 710

Cyclopropanecarboxamide, N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]-N-(2-methylpropyl)- 711

Cyclopropanecarboxamide, N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]-N-methyl- 712

Cyclopropanecarboxamide, N-ethyl-N- [(2-methyl-2-phenyl-cyclopropyl)- methyl]- 713

Cyclopropanecarboxamide, N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]-N-propyl- 714

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]- 715

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-methyl-2- phenyl-cyclopropyl)-methyl]- 716

Cyclopropanecarboxamide, N-ethenyl- N-[(2-methyl-2-phenyl-cyclopropyl)- methyl]- 717

Cyclopropanecarboxamide, N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]-N-(2-propenyl)- 718

Cyclopropanecarboxamide, N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]-N-(cyclopropylmethyl)- 719

Cyclopropanecarboxamide, N-butyl-N- [(2-methyl-2-phenyl-cyclopropyl)- methyl]- 720

Cyclopropanecarboxamide, N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]-N-(2-methylpropyl)- 721

Cyclopropanecarboxamide, N-[(1- methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]-N-methyl- 722

Cyclopropanecarboxamide, N-ethyl-N- [(1-methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]- 723

Cyclopropanecarboxamide, N-[(1- methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]-N-propyl- 724

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(1-methyl-2-[(3Z)- 3-hexenyl]-cyclopropyl)-methyl]- 725

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(1-methyl-2- [(3Z)-3-hexenyl]-cyclopropyl)- methyl]- 726

Cyclopropanecarboxamide, N-ethenyl- N-[(1-methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]- 727

Cyclopropanecarboxamide, N-[(1- methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]-N-(2- propenyl)- 728

Cyclopropanecarboxamide, N-[(1- methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl)-N- (cyclopropylmethyl)- 729

Cyclopropanecarboxamide, N-butyl-N- [(1-methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]- 730

Cyclopropanecarboxamide, N-[(1- methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]-N-(2- methylpropyl)- 731

Cyclopropanecarboxamide, N-[(1- methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]-N-methyl- 732

Cyclopropanecarboxamide, N-ethyl-N- [(1-methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]- 733

Cyclopropanecarboxamide, N-[(1- methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]-N-propyl- 734

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(1-methyl-2-[(3Z)- 3-hexenyl]-cyclopropyl)-methyl]- 735

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(1-methyl-2- [(3Z)-3-hexenyl]-cyclopropyl)- methyl]- 736

Cyclopropanecarboxamide, N-ethenyl- N-[(1-methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]- 737

Cyclopropanecarboxamide, N-[(1- methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]-N-(2- propenyl)- 738

Cyclopropanecarboxamide, N-[(1- methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 739

Cyclopropanecarboxamide, N-butyl-N- [(1-methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]- 740

Cyclopropanecarboxamide, N-[(1- methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]-N-(2- methylpropyl)- 741

Cyclopropanecarboxamide, N-[(2- phenyl-cyclopropyl)-methyl]-N- methyl- 742

Cyclopropanecarboxamide, N-ethyl-N- [(2-phenyl-cyclopropyl)-methyl]- 743

Cyclopropanecarboxamide, N-[(2- phenyl-cyclopropyl)-methyl]-N- propyl- 744

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-phenyl- cyclopropyl)-methyl]- 745

Cyclopropanecarboxamide, N-(1,1- dimethyletlyl)-N-[(2-phenyl- cyclopropyl)-methyl]- 746

Cyclopropanecarboxamide, N-ethenyl- N-[(2-methyl-2-phenyl-cyclopropyl)- methyl]- 747

Cyclopropanecarboxamide, N-[(2- phenyl-cyclopropyl)-methyl]-N-(2- propenyl)- 748

Cyclopropanecarboxamide, N-[(2- phenyl-cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 749

Cyclopropanecarboxamide, N-butyl-N- [(2-phenyl-cyclopropyl)-methyl]- 750

Cyclopropanecarboxamide, N-[(2- phenyl-cyclopropyl)-methyl]-N-(2- methylpropyl)- 751

Cyclopropanecarboxamide, N-[(2- phenyl-cyclopropyl)-methyl]-N- methyl- 752

Cyclopropanecarboxamide, N-ethyl-N- [(2-phenyl-cyclopropyl)-methyl]- 753

Cyclopropanecarboxamide, N-[(2- phenyl-cyclopropyl)-methyl]-N- propyl- 754

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-phenyl- cyclopropyl)-methyl]- 755

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-phenyl- cyclopropyl)-methyl]- 756

Cyclopropanecarboxamide, N-ethenyl- N-[(2-methyl-2-phenyl-cyclopropyl)- methyl]- 757

Cyclopropanecarboxamide, N-[(2- phenyl-cyclopropyl)-methyl]-N-(2- propenyl)- 758

Cyclopropanecarboxamide, N-[(2- phenyl-cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 759

Cyclopropanecarboxamide, N-butyl-N- [(2-phenyl-cyclopropyl)-methyl]- 760

Cyclopropanecarboxamide, N-[(2- phenyl-cyclopropyl)-methyl]-N-(2- methylpropyl)- 761

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-methyl-2,2-dimethyl- 762

Propanamide, N-ethyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2,2-dimethyl- 763

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-propyl-2,2-dimethyl- 764

Propanamide, N-(1-methylethyl)-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2,2-dimethyl- 765

Propanamide, N-(1,1-dimethylethyl)- N-[(2-methyl-2-[4-methyl-3- pentenyl]-cyclopropyl)-methyl]-2,2- dimethyl- 766

Propanamide, N-ethenyl-N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2,2-dimethyl- 767

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-propenyl)-2,2- dimethyl- 768

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)-2,2- dimethyl- 769

Propanamide, N-butyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2,2-dimethyl- 770

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-methylpropyl)-2,2- dimethyl- 771

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-methyl-2,2-dimethyl- 772

Propanamide, N-ethyl-N-[(2-methyl- 2-(4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2,2-dimethyl- 773

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-propyl-2,2-dimethyl- 774

Propanamide, N-(1-methylethyl)-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2,2-dimethyl- 775

Propanamide, N-(1,1-dimethylethyl)- N-[(2-methyl-2-[4-methyl-3- pentenyl]-cyclopropyl)-methyl]-2,2- dimethyl- 776

Propanamide, N-ethenyl-N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2,2-dimethyl- 777

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-propenyl)-2,2- dimethyl- 778

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)-2,2- dimethyl- 779

Propanamide, N-butyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2,2-dimethyl- 780

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-methylpropyl)-2,2- dimethyl- 781

Butanamide, N-[(2-methyl-2-(4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-methyl- 782

Butanamide, N-ethyl-N-[(2-methyl-2- [4-methyl-3-pentenyl]-cyclopropyl)- methyl]- 783

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-propyl- 784

Butanamide, N-(1-methylethyl)-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 785

Butanamide, N-(1,1-dimethylethyl)- N-[(2-methyl-2-[4-methyl-3- pentenyl]-cyclopropyl)-methyl]- 786

Butanamide, N-ethenyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 787

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-propenyl)- 788

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)- 789

Butanamide, N-butyl-N-[(2-methyl-2- [4-methyl-3-pentenyl]-cyclopropyl)- methyl]- 790

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-methylpropyl)- 791

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-methyl- 792

Butanamide, N-ethyl-N-[(2-methyl-2- [4-methyl-3-pentenyl]-cyclopropyl)- methyl]- 793

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-propyl- 794

Butanamide, N-(1-methylethyl)-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 795

Butanamide, N-(1,1-dimethylethyl)- N-[(2-methyl-2-[4-methyl-3- pentenyl]-cyclopropyl)-methyl]- 796

Butanamide, N-ethenyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 797

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-propenyl)- 798

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)- 799

Butanamide, N-butyl-N-[(2-methyl-2- [4-methyl-3-pentenyl]-cyclopropyl)- methyl]- 800

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-methylpropyl)- 801

Propanamide; N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-methyl- 802

Propanamide, N-ethyl-N-[(1-methyl- 2-phenyl-cyclopropyl)-methyl]- 803

Propanamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-propyl- 804

Propanamide, N-(1-methylethyl)-N- [(1-methyl-2-phenyl-cyclopropyl)- methyl]- 805

Propanamide, N-(1,1-dimethylethyl)- N-[(1-methyl-2-phenyl-cyclopropyl)- methyl]- 806

Propanamide, N-ethenyl-N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]- 807

Propanamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- propenyl)- 808

Propanamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 809

Propanamide, N-butyl-N-[(1-methyl- 2-phenyl-cyclopropyl)-methyl]- 810

Propanamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- methylpropyl)- 811

Propanamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-methyl- 812

Propanamide, N-ethyl-N-[(1-methyl- 2-phenyl-cyclopropyl)-methyl]- 813

Propanamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-propyl- 814

Propanamide, N-(1-methylethyl)-N- [(1-methyl-2-phenyl-cyclopropyl)- methyl]- 815

Propanamide, N-(1,1-dimethylethyl)- N-[(1-methyl-2-phenyl-cyclopropyl)- methyl]- 816

Propanamide, N-ethenyl-N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]- 817

Propanamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- propenyl)- 818

Propanamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 819

Propanamide, N-butyl-N-[(1-methyl- 2-phenyl-cyclopropyl)-methyl]- 820

Propanamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- methylpropyl)- 821

Propanamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-methyl- 822

Propanamide, N-ethyl-N-[(2-methyl- 2-phenyl-cyclopropyl)-methyl]- 823

Propanamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-propyl- 824

Propanamide, N-(1-methylethyl)-N- [(2-methyl-2-phenyl-cyclopropyl)- methyl]- 825

Propanamide, N-(1,1-dimethylethyl)- N-[(2-methyl-2-phenyl-cyclopropyl)- methyl]- 826

Propanamide, N-ethenyl-N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]- 827

Propanamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- propenyl)- 828

Propanamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 829

Propanamide, N-butyl-N-[(2-methyl- 2-phenyl-cyclopropyl)-methyl]- 830

Propanamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- methylpropyl)- 831

Propanamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl)-N-methyl- 832

Propanamide, N-ethyl-N-[(2-methyl- 2-phenyl-cyclopropyl)-methyl]- 833

Propanamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-propyl- 834

Propanamide, N-(1-methylethyl)-N- [(2-methyl-2-phenyl-cyclopropyl)- methyl]- 835

Propanamide, N-(1,1-dimethylethyl)- N-[(2-methyl-2-phenyl-cyclopropyl)- methyl]- 836

Propanamide, N-ethenyl-N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]- 837

Propanamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- propenyl)- 838

Propanamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 839

Propanamide, N-butyl-N-[(2-methyl- 2-phenyl-cyclopropyl)-methyl]- 840

Propanamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- methylpropyl)- 841

Acetamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-methyl- 842

Acetamide, N-ethyl-N-[(1-methyl-2- phenyl-cyclopropyl)-methyl]- 843

Acetamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-propyl- 844

Acetamide, N-(1-methylethyl)-N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]- 845

Acetamide, N-(1,1-dimethylethyl)-N- [(1-methyl-2-phenyl-cyclopropyl)- methyl]- 846

Acetamide, N-ethenyl-N-[(1-methyl- 2-phenyl-cyclopropyl)-methyl]- 847

Acetamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- propenyl)- 848

Acetamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 849

Acetamide, N-butyl-N-[(1-methyl-2- phenyl-cyclopropyl)-methyl]- 850

Acetamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- methylpropyl)- 851

Acetamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-methyl- 852

Acetamide, N-ethyl-N-[(1-methyl-2- phenyl-cyclopropyl)-methyl]- 853

Acetamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-propyl- 854

Acetamide, N-(1-methylethyl)-N-[(1- methyl-2-phenyl-cyclopropyl)- methyl]- 855

Acetamide, N-(1,1-dimethylethyl)-N- [(1-methyl-2-phenyl-cyclopropyl)- methyl]- 856

Acetamide, N-ethenyl-N-[(1-methyl- 2-phenyl-cyclopropyl)-methyl]- 857

Acetamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl)-N-(2- propenyl)- 858

Acetamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 859

Acetamide, N-butyl-N-[(1-methyl-2- phenyl-cyclopropyl)-methyl]- 860

Acetamide, N-[(1-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- methylpropyl)- 861

Acetamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-methyl- 862

Acetamide, N-ethyl-N-[(2-methyl-2- phenyl-cyclopropyl)-methyl]- 863

Acetamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-propyl- 864

Acetamide, N-(1-methylethyl)-N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]- 865

Acetamide, N-(1,1-dimethylethyl)-N- [(2-methyl-2-phenyl-cyclopropyl)- methyl]- 866

Acetamide, N-ethenyl-N-[(2-methyl- 2-phenyl-cyclopropyl)-methyl]- 867

Acetamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl)-N-(2- propenyl)- 868

Acetamide, N-[(2-methyl-2-phenyl- cycloprapyl)-methyl]-N- (cyclopropylmethyl)- 869

Acetamide, N-butyl-N-[(2-methyl-2- phenyl-cyclopropyl)-methyl)- 870

Acetamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- methylpropyl)- 871

Acetamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-methyl- 872

Acetamide, N-ethyl-N-[(2-methyl-2- phenyl-cyclopropyl)-methyl]- 873

Acetamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-propyl- 874

Acetamide, N-(1-methylethyl)-N-[(2- methyl-2-phenyl-cyclopropyl)- methyl]- 875

Acetamide, N-(1,1-dimethylethyl)-N- [(2-methyl-2-phenyl-cyclopropyl)- methyl]- 876

Acetamide, N-ethenyl-N-[(2-methyl- 2-phenyl-cyclopropyl)-methyl]- 877

Acetamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N-(2- propenyl)- 878

Acetamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 879

Acetamide, N-butyl-N-[(2-methyl-2- phenyl-cyclopropyl)-methyl]- 880

Acetamide, N-[(2-methyl-2-phenyl- cyclopropyl)-methyl)]N-(2- methylpropyl)- 881

Acetamide, N-[(1-methyl-2-[(3Z)-3- hexenyl]-cyclopropyl)-methyl]-N- methyl- 882

Acetamide, N-ethyl-N-[(1-methyl-2- [(3Z)-3-hexenyl]-cyclopropyl)- methyl]- 883

Acetamide, N-[(1-methyl-2-[(3Z)-3- hexenyl]-cyclopropyl)-methyl]-N- propyl- 884

Acetamide, N-(1-methylethyl)-N-[(1- methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]- 885

Acetamide, N-(1,1-dimethylethyl)-N- [(1-methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]- 886

Acetamide, N-ethenyl-N-[(1-methyl- 2-[(3Z)-3-hexenyl]-cyclopropyl)- methyl]- 887

Acetamide, N-[(1-methyl-2-[(3Z)-3- hexenyl]-cyclopropyl)-methyl]-N-(2- propenyl)- 888

Acetamide, N-[(1-methyl-2-[(3Z)-3- hexenyl]-cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 889

Acetamide, N-butyl-N-[(1-methyl-2- [(3Z)-3-hexenyl]-cyclopropyl)- methyl]- 890

Acetamide, N-[(1-methyl-2-[(3Z)-3- hexenyl]-cyclopropyl)-methyl]-N-(2- methylpropyl)- 891

Acetamide, N-[(1-methyl-2-[(3Z)-3- hexenyl]-cyclopropyl)-methyl]-N- methyl- 892

Acetamide, N-ethyl-N-[(1-methyl-2- [(3Z)-3-hexenyl]-cyclopropyl)- methyl]- 893

Acetamide, N-[(1-methyl-2-(3Z)-3- hexenyl]-cyclopropyl)-methyl]-N- propyl- 894

Acetamide, N-(1-methylethyl)-N-[(1- methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]- 895

Acetamide, N-(1,1-dimethylethyl)-N- [(1-methyl-2-[(3Z)-3-hexenyl]- cyclopropyl)-methyl]- 896

Acetamide, N-ethenyl-N-[(1-methyl- 2-[(3Z)-3-hexenyl]-cyclopropyl)- methyl]- 897

Acetamide, N-[(1-methyl-2-[(3Z)-3- hexenyl]-cyclopropyl)-methyl]-N-(2- propenyl)- 898

Acetamide, N-[(1-methyl-2-[(3Z)-3- hexenyl]-cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 899

Acetamide, N-butyl-N-[(1-methyl-2- [(3Z)-3-hexenyl]-cyclopropyl)- methyl]- 900

Acetamide, N-[(1-methyl-2-[(3Z)-3- hexenyl]-cyclopropyl)-methyl)-N-(2- methylpropyl)- 901

Propanamide, N-[(2-[3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-methyl- 902

Propanamide, N-ethyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 903

Propanamide, N-[(2-[3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-propyl- 904

Propanamide, N-(1-methylethyl)-N- [(2-[3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 905

Propanamide, N-(1,1-dimethylethyl)- N-[(2-[3-cyclohexen-1-yl)- cyclopropyl)-methyl]- 906

Propanamide, N-ethenyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 907

Propanamide, N-[(2-[3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-(2- propenyl)- 908

Propanamide, N-[(2-[3-cyclohexen-1- yl]-cyclopropyl)-methyl)-N- (cyclopropylmethyl)- 909

Propanamide, N-butyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 910

Propanamide, N-[(2-[3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-(2- methylpropyl)- 911

Propanamide, N-[(2-[3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-methyl- 912

Propanamide, N-ethyl-N-[(2-[3- cyclohexen-1-yl cyclopropyl)- methyl]- 913

Propanamide, N-[(2-[3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-propyl- 914

Propanamide, N-(1-methylethyl)-N- [(2-[3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 915

Propanamide, N-(1,1-dimethylethyl)- N-[(2-[3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 916

Propanamide, N-ethenyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 917

Propanamide, N-[(2-[3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-(2- propenyl)- 918

Propanamide, N-[(2-[3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 919

Propanamide, N-butyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 920

Propanamide, N-[(2-(3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-(2- methylpropyl)- 921

Acetamide, N-[(2-[3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-methyl- 922

Acetamide, N-ethyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 923

Acetamide, N-[(2-[3-cyclohexen-1- yl]-cycloprapyl)-methyl]-N-propyl- 924

Acetamide, N-(1-methylethyl)-N-[(2- [3-cyclohexen-1-yl]-cyclopropyl)- methyl]- 925

Acetamide, N-(1,1-dimethylethyl)-N- [(2-[3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 926

Acetamide, N-ethenyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 927

Acetamide, N-[(2-[3-cyclohexenyl]- cyclopropyl)-methyl]-N-(2- propenyl)- 928

Acetamide, N-[(2-(3-cyclohexenyl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 929

Acetamide, N-butyl-N-[(2-[3- cyclohexenyl cyclooctenyl]- cyclopropyl)-methyl]- 930

Acetamide, N-[(2-[3-cyclohexenyl]- cyclopropyl)-methyl]-N-(2- methylpropyl)- 931

Acetamide, N-[(2-(3-cyclohexenyl]- cyclopropyl)-methyl]-N-methyl- 932

Acetamide, N-ethyl-N-[(2-[3- cyclohexenyl]-cyclopropyl)-methyl]- 933

Acetamide, N-[(2-[3-cyclohexenyl]- cyclopropyl)-methyl]-N-propyl- 934

Acetamide, N-(1-methylethyl)-N-[(2- [3-cyclohexen-1-yl]-cyclopropyl)- methyl]- 935

Acetamide, N-(1,1-dimethylethyl)-N- [(2-[3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 936

Acetamide, N-ethenyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 937

Acetamide, N-[(2-[3-cyclohexenyl]- cyclopropyl)-methyl]-N-(2- propenyl)- 938

Acetamide, N-[(2-[3-cyclohexenyl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 939

Acetamide, N-butyl-N-[(2-[3- cyclohexenyl cyclooctenyl]- cyclopropyl)-methyl]- 940

Acetamide, N-[(2-[3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-(2- methylpropyl)- 941

Propanamide, N-[(2-[3- cyclohexenyl]-cyclopropyl)-methyl]- N-methyl-2,2-dimethyl- 942

Propanamide, N-ethyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-2,2-dimethyl- 943

Propanamide, N-[(2-[3- cyclohexenyl]-cyclopropyl)-methyl]- N-propyl-2,2-dimethyl- 944

Propanamide, N-(1-methylethyl)-N- [(2-[3-cyclohexen-1-yl cyclopropyl)-methyl]-2,2-dimethyl- 945

Propanamide, N-(1,1-dimethylethyl)- N-[(2-[3-cyclohexenyl]- cyclopropyl)-methyl]-2,2-dimethyl- 946

Propanamide, N-ethenyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-2,2-dimethyl- 947

Propanamide, N-[(2-[3- cyclohexenyl]-cyclopropyl)-methyl]- N-(2-propenyl)-2,2-dimethyl- 948

Propanamide, N-[(2-[3- cyclohexenyl]-cyclopropyl)-methyl]- N-(cyclopropylmethyl)-2,2-dimethyl- 949

Propanamide, N-butyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-2,2-dimethyl- 950

Propanamide, N-[(2-[3- cyclohexenyl]-cyclopropyl)-methyl]- N-(2-methylpropyl)-2,2-dimethyl- 951

Propanamide, N-[(2-[3- cyclohexenyl]-cyclopropyl)-methyl]- N-methyl-2,2-dimethyl- 952

Propanamide, N-ethyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-2,2-dimethyl- 953

Propanamide, N-[(2-[3-cyclohexenyl- cyclooctenyl]-cyclopropyl)-methyl]- N-propyl-2,2-dimethyl- 954

Propanamide, N-(1-methylethyl)-N- [(2-[3-cyclohexen-1-yl]- cyclopropyl)-methyl]-2,2-dimethyl- 955

Propanamide, N-(1,1-dimethylethyl)- N-[(2-[3-cyclooctenyl]- cyclopropyl)-methyl]-2,2-dimethyl- 956

Propanamide, N-ethenyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-2,2-dimethyl- 957

Propanamide, N-[(2-[3- cyclohexenyl]-cyclopropyl)-methyl]- N-(2-propenyl)-2,2-dimethyl- 958

Propanamide, N-[(2-[3- cyclohexenyl]-cyclopropyl)-methyl]- N-(cyclopropylmethyl)-2,2-dimethyl- 959

Propanamide, N-butyl-N-[(2-[3- cyclohexen-1-yl]-cyclopropyl)- methyl]-2,2-dimethyl- 960

Propanamide, N-[(2-[3- cyclohexenyl]-cyclopropyl)-methyl]- N-(2-methylpropyl)-2,2-dimethyl- 961

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-methyl-2-methyl- 962

Butanamide, N-ethyl-N-[(2-methyl-2- [4-methyl-3-pentenyl]-cyclopropyl)- methyl]-2-methyl- 963

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-propyl-2-methyl- 964

Butanamide, N-(1-methylethyl)-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2-methyl- 965

Butanamide, N-(1,1-dimethylethyl)- N-[(2-methyl-2-[4-methyl-3- pentenyl]-cyclopropyl)-methyl]-2- methyl- 966

Butanamide, N-ethenyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2-methyl- 967

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-propenyl)-2-methyl- 968

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)-2- methyl- 969

Butanamide, N-butyl-N-[(2-methyl-2- [4-methyl-3-pentenyl]-cyclopropyl)- methyl]-2-methyl- 970

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-methylpropyl)-2- methyl- 971

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-methyl-2-methyl- 972

Butanamide, N-ethyl-N-(2-methyl-2- [4-methyl-3-pentenyl]-cyclopropyl)- methyl]-2-methyl- 973

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-propyl-2-methyl- 974

Butanamide, N-(1-methylethyl)-N- [(2-methyl-2-(4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2-methyl- 975

Butanamide, N-(1,1-dimethylethyl)- N-[(2-methyl-2-[4-methyl-3- pentenyl]-cyclopropyl)-methyl]-2- methyl- 976

Butanamide, N-ethenyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2-methyl- 977

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-propenyl)-2-methyl- 978

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)-2- methyl- 979

Butanamide, N-butyl-N-[(2-methyl-2- [4-methyl-3-pentenyl]-cyclopropyl)- methyl]-2-methyl- 980

Butanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-methylpropyl)-2- methyl- 981

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-N-methyl- 982

Cyclopropanecarboxamide, N-ethyl-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 983

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-N-propyl- 984

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]- 985

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]- 986

Cyclopropanecarboxamide, N-ethenyl- N-[(2-methyl-2-[4-methyl-3- pentenyl]-cyclopropyl)-methyl]- 987

Cyclopropanecarboxamide, N-[(2- methyl-2-(4-methyl-3-pentenyl]- cyclopropyl)-methyl]-N-(2- propenyl)- 988

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 989

Cyclopropanecarboxamide, N-butyl-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 990

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-N-(2- methylpropyl)- 991

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-N-methyl- 992

Cyclopropanecarboxamide, N-ethyl-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 993

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-N-propyl- 994

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]- 995

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]- 996

Cyclopropanecarboxamide, N-ethenyl- N-[(2-methyl-2-[4-methyl-3- pentenyl]-cyclopropyl)-methyl]- 997

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-N-(2- propenyl)- 998

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 999

Cyclopropanecarboxamide, N-butyl-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 1000

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-N-(2- methylpropyl)- 1001

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-methyl-2-methyl- 1002

Propanamide, N-ethyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2-methyl- 1003

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-propyl-2-methyl- 1004

Propanamide, N-(1-methylethyl)-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2-methyl- 1005

Propanamide, N-(1,1-dimethylethyl)- N-[(2-methyl-2-[4-methyl-3- pentenyl]-cyclopropyl)-methyl]-2- methyl- 1006

Propanamide, N-ethenyl-N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2-methyl- 1007

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-propenyl)-2-methyl- 1008

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)-2- methyl- 1009

Propanamide, N-butyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl)-2-methyl- 1010

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-methylpropyl)-2- methyl- 1011

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-methyl-2-methyl- 1012

Propanamide, N-ethyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2-methyl- 1013

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-propyl-2-methyl- 1014

Propanamide, N-(1-methylethyl)-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2-methyl- 1015

Propanamide, N-(1,1-dimethylethyl)- N-[(2-methyl-2-[4-methyl-3- pentenyl]-cyclopropyl)-methyl]-2- methyl- 1016

Propanamide, N-ethenyl-N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2-methyl- 1017

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-propenyl)-2-methyl- 1018

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)-2- methyl- 1019

Propanamide, N-butyl-N-[(2-methyl- 2-(4-methyl-3-pentenyl]- cyclopropyl)-methyl]-2-methyl- 1020

Propanamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-methylpropyl)-2- methyl- 1021

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-methyl- 1022

2-butenamide, N-ethyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 1023

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-propyl- 1024

2-butenamide, N-(1-methylethyl)-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 1025

2-butenamide, N-(1,1- dimethylethyl)-N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]- 1026

2-butenamide, N-ethenyl-N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 1027

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-propenyl)- 1028

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)- 1029

2-butenamide, N-butyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 1030

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-methylpropyl)- 1031

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-methyl- 1032

2-butenamide, N-ethyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 1033

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-propyl- 1034

2-butenamide, N-(1-methylethyl)-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 1035

2-butenamide, N-(1,1- dimethylethyl)-N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]- 1036

2-butenamide, N-ethenyl-N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 1037

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-propenyl)- 1038

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl)-N-(cyclopropylmethyl)- 1039

2-butenamide, N-butyl-N-[(2-methyl- 2-(4-methyl-3-pentenyl]- cyclopropyl)-methyl]- 1040

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-methylpropyl)- 1041

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-methyl-3-methyl- 1042

2-butenamide, N-ethyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-3-methyl- 1043

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-propyl-3-methyl- 1044

2-butenamide, N-(1-methylethyl)-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-3-methyl- 1045

2-butenamide, N-(1,1- dimethylethyl)-N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-3-methyl- 1046

2-butenamide, N-ethenyl-N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-3-methyl- 1047

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-propenyl)-3-methyl- 1048

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)-3- methyl- 1049

2-butenamide, N-butyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-3-methyl- 1050

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-methylpropyl)-3- methyl- 1051

2-butenamide, N-[(2-methyl-2-(4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-methyl-3-methyl- 1052

2-butenamide, N-ethyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-3-methyl- 1053

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-propyl-3-methyl- 1054

2-butenamide, N-(1-methylethyl)-N- [(2-methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-3-methyl- 1055

2-butenamide, N-(1,1- dimethylethyl)-N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-3-methyl- 1056

2-butenamide, N-ethenyl-N-[(2- methyl-2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-3-methyl- 1057

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-propenyl)-3-methyl- 1058

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)-3- methyl- 1059

2-butenamide, N-butyl-N-[(2-methyl- 2-[4-methyl-3-pentenyl]- cyclopropyl)-methyl]-3-methyl- 1060

2-butenamide, N-[(2-methyl-2-[4- methyl-3-pentenyl]-cyclopropyl)- methyl]-N-(2-methylpropyl)-3- methyl- 1061

Cyclopropanecarboxamide, N-[(2-[3Z- nonenyl]-cyclopropyl)-methyl]-N- methyl 1062

Cyclopropanecarboxamide, N-ethyl-N- [2-[3Z-nonenyl]-cyclopropyl)- methyl]- 1063

Cyclopropanecarboxamide, N-[(2-[3Z- nonenyl]-cyclopropyl)-methyl]-N- propyl- 1064

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-[3Z-nonenyl]- cyclopropyl)-methyl]- 1065

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-[3Z-nonenyl]- cyclopropyl)-methyl]- 1066

Cyclopropanecarboxamide, N-ethenyl- N-[(2-[3Z-nonenyl]-cyclopropyl)- methyl]- 1067

Cyclopropanecarboxamide, N-[(2-[3Z- nonenyl]-cyclopropyl)-methyl]-N-(2- propenyl)- 1068

Cyclopropanecarboxamide, N-[(2-[3Z- nonenyl]-cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1069

Cyclopropanecarboxamide, N-butyl-N- [(2-[3Z-nonenyl]-cyclopropyl)- methyl]- 1070

Cyclopropanecarboxamide, N-[(2-[3Z- nonenyl]-cyclopropyl)-methyl]-N-(2- methylpropyl)- 1071

Cyclopropanecarboxamide, N-[(2-[3Z- nonenyl]-cyclopropyl)-methyl]-N- methyl- 1072

Cyclopropanecarboxamide, N-ethyl-N- [(2-[3Z-nonenyl]-cyclopropyl)- methyl]- 1073

Cyclopropanecarboxamide, N-[(2-[3Z- nonenyl]-cyclopropyl)-methyl]-N- propyl- 1074

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-f3Z-nonenyl]- cyclopropyl)-methyl]- 1075

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-[3Z-nonenyl]- cyclopropyl)-methyl]- 1076

Cyclopropanecarboxamide, N-ethenyl- N-[(2-[3Z-nonenyl]-cyclopropyl)- methyl]- 1077

Cyclopropanecarboxamide, N-[(2-[3Z- nonenyl]-cyclopropyl)-methyl]-N-(2- propenyl)- 1078

Cyclopropanecarboxamide, N-[(2-[3Z- nonenyl]-cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1079

Cyclopropanecarboxamide, N-butyl-N- [(2-[3Z-nonenyl]-cyclopropyl)- methyl]- 1080

Cyclopropanecarboxamide, N-[(2-[3Z- nonenyl]-cyclopropyl)-methyl]-N-(2- methylpropyl)- 1081

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-methyl- 1082

Cyclopropanecarboxamide, N-ethyl-N- [(2-methyl-2-[4-methyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 1083

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl)-N-propyl- 1084

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1085

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1086

Cyclopropanecarboxamide, N-ethenyl- N-[(2-methyl-2-[4-methyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 1087

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-(2- propenyl)- 1088

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1089

Cyclopropanecarboxamide, N-butyl-N- [(2-methyl-2-[4-methyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 1090

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-(2- methylpropyl)- 1091

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-methyl- 1092

Cyclopropanecarboxamide, N-ethyl-N- [(2-methyl-2-[4-methyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 1093

Cyclopropanecarboxamide, N-[(2- methyl-2-(4-methyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-propyl- 1094

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-methyl-2-(4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1095

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1096

Cyclopropanecarboxamide, N-ethenyl- N-[(2-methyl-2-[4-methyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 1097

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-(2- propenyl)- 1098

Cyclopropanecarboxamide, N-[(2- methyl-2-(4-methyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1099

Cyclopropanecarboxamide, N-butyl-N- [(2-methyl-2-[4-methyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 1100

Cyclopropanecarboxamide, N-[(2- methyl-2-[4-methyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]-N-(2- methylpropyl)- 1101

Cyclopropanecarboxamide, N-[(2,2- dimethyl-cyclopropyl)-methyl]-N- methyl- 1102

Cyclopropanecarboxamide, N-ethyl-N- [(2,2-dimethyl-cyclopropyl)- methyl]- 1103

Cyclopropanecarboxamide, N-[(2,2- dimethyl-cyclopropyl)-methyl]-N- propyl- 1104

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2,2-dimethyl- cyclopropyl)-methyl]- 1105

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2,2-dimethyl- cyclopropyl)-methyl]- 1106

Cyclopropanecarboxamide, N-ethenyl- N-[(2,2-dimethyl-cyclopropyl)- methyl]- 1107

Cyclopropanecarboxamide, N-[(2,2- dimethyl-cyclopropyl)-methyl]-N-(2- propenyl)- 1108

Cyclopropanecarboxamide, N-[(2,2- dimethyl-cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1109

Cyclopropanecarboxamide, N-butyl-N- [(2,2-dimethyl-cyclopropyl)- methyl]- 1110

Cyclopropanecarboxamide, N-[(2,2- dimethyl-cyclopropyl)-methyl]-N-(2- methylpropyl)- 1111

Cyclopropanecarboxamide, N-[(2- [2,4-dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-methyl- 1112

Cyclopropanecarboxamide, N-ethyl-N- [(2-[2,4-dimethyl-3-cyclohexen-1- yl]-propyl)-methyl- 1113

Cyclopropanecarboxamide, N-[(2- [2,4-dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-propyl- 1114

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-[2,4-dimethyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 1115

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-[2,4-dimethyl- 3-cyclohexen-1-yl]-cyclopropyl)- methyl]- 1116

Cyclopropanecarboxamide, N-ethenyl- N-[(2-[2,4-dimethyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]- 1117

Cyclopropanecarboxamide, N-[(2- [2,4-dimethyl-3-cyclohexen-1-yl]- propyl)-methyl]-N-(2-propenyl)- 1118

Cyclopropanecarboxamide, N-[(2- [2,4-dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1119

Cyclopropanecarboxamide, N-butyl-N- [(2-[2,4-dimethyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]- 1120

Cyclopropanecarboxamide, N-[(2- [2,4-dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-(2- methylpropyl)- 1121

Cyclopropanecarboxamide, N-[(2- [2,4-dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-methyl- 1122

Cyclopropanecarboxamide, N-ethyl-N- [(2-[2,4-dimethyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]- 1123

Cyclopropanecarboxamide, N-[(2- [2,4-dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-propyl- 1124

Cyclopropanecarboxamide, N-(1- methylethyl)-N-[(2-[2,4-dimethyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 1125

Cyclopropanecarboxamide, N-(1,1- dimethylethyl)-N-[(2-[2,4-dimethyl- 3-cyclohexen-1-yl]-cyclopropyl)- methyl]- 1126

Cyclopropanecarboxamide, N-ethenyl- N-[(2-[2,4-dimethyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]- 1127

Cyclopropanecarboxamide, N-[(2- [2,4-dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-(2- propenyl)- 1128

Cyclopropanecarboxamide, N-[(2- [2,4-dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1129

Cyclopropanecarboxamide, N-butyl-N- [(2-[2,4-dimethyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]- 1130

Cyclopropanecarboxamide, N-[(2- [2,4-dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-(2- methylpropyl)- 1131

Acetamide, N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-methyl- 1132

Acetamide, N-ethyl-N-[(2-methyl-2- [4-methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1133

Acetamide, N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl)-N-propyl- 1134

Acetamide, N-(1-methylethyl)-N-[(2- methyl-2-(4-methyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]- 1135

Acetamide, N-(1,1-dimethylethyl)-N- [(2-methyl-2-[4-methyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 1136

Acetamide, N-ethenyl-N-[(2-methyl- 2-[4-methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1137

Acetamide, N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-(2- propenyl)- 1138

Acetamide, N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1139

Acetamide, N-butyl-N-[(2-methyl-2- [4-methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1140

Acetamide, N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-(2- methylpropyl)- 1141

Acetamide, N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-methyl- 1142

Acetamide, N-ethyl-N-[(2-methyl-2- [4-methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1143

Acetamide, N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-propyl- 1144

Acetamide, N-(1-methylethyl)-N-[(2- methyl-2-[4-methyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]- 1145

Acetamide, N-(1,1-dimethylethyl)-N- [(2-methyl-2-[4-methyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]- 1146

Acetamide, N-ethenyl-N-[(2-methyl- 2-[4-methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1147

Acetamide, N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-(2- propenyl)- 1148

Acetamide, N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1149

Acetamide, N-butyl-N-[(2-methyl-2- [4-methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1150

Acetamide, N-[(2-methyl-2-[4- methyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]-N-(2- methylpropyl)- 1151

Acetamide, N-[(2-[2,4-dimethyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-methyl- 1152

Acetamide, N-ethyl-N-[(2-[2,4- dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1153

Acetamide, N-[(2-[2,4-dimethyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-propyl- 1154

Acetamide, N-(1-methylethyl)-N-[(2- [2,4-dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1155

Acetamide, N-(1,1-dimethylethyl)-N- [(2-[2,4-dimethyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]- 1156

Acetamide, N-ethenyl-N-[(2-[2,4- dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1157

Acetamide, N-[(2-[2,4-dimethyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-(2-propenyl)- 1158

Acetamide, N-[(2-[2,4-dimethyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)- 1159

Acetamide, N-butyl-N-[(2-[2,4- dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1160

Acetamide, N-[(2-[2,4-dimethyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-(2-methylpropyl)- 1161

Acetamide, N-[(2-[2,4-dimethyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-methyl- 1162

Acetamide, N-ethyl-N-[(2-[2,4- dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1163

Acetamide, N-[(2-[2,4-dimethyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-propyl- 1164

Acetamide, N-(1-methylethyl)-N-[(2- [2,4-dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1165

Acetamide, N-(1,1-dimethylethyl)-N- [(2-[2,4-dimethyl-3-cyclohexen-1- yl]-cyclopropyl)-methyl]- 1166

Acetamide, N-ethenyl-N-[(2-[2,4- dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1167

Acetamide, N-[(2-[2,4-dimethyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-(2-propenyl)- 1168

Acetamide, N-[(2-[2,4-dimethyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-(cyclopropylmethyl)- 1169

Acetamide, N-butyl-N-[(2-[2,4- dimethyl-3-cyclohexen-1-yl]- cyclopropyl)-methyl]- 1170

Acetamide, N-[(2-[2,4-dimethyl-3- cyclohexen-1-yl]-cyclopropyl)- methyl]-N-(2-methylpropyl)- 1171

Propanamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-methyl- 1172

Propanamide, N-ethyl-N-[(2-[3Z- hexenyl]-cyclopropyl)-methyl]- 1173

Propanamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-propyl- 1174

Propanamide, N-(1-methylethyl)-N- [(2-[3Z-hexenyl]-cyclopropyl)- methyl]- 1175

Propanamide, N-(1,1-dimethylethyl)- N-[(2-[3Z-hexenyl]-cyclopropyl)- methyl]- 1176

Propanamide, N-ethenyl-N-[(2-[3Z- hexenyl]-cyclopropyl)-methyl]- 1177

Propanamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-(2- propenyl)- 1178

Propanamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1179

Propanamide, N-butyl-N-[2-[3Z- hexenyl]-cyclopropyl)-methyl]- 1180

Propanamide, N-[(2-[3Z-hexenyl)- cyclopropyl)-methyl]-N-(2- methylpropyl)- 1181

Propanamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-methyl- 1182

Propanamide, N-ethyl-N-[(2-[3Z- hexenyl]-cyclopropyl)-methyl]- 1183

Propanamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-propyl- 1184

Propanamide, N-(1-methylethyl)-N- [(2-[3Z-hexenyl]-cyclopropyl)- methyl]- 1185

Propanamide, N-(1,1-dimethylethyl)- N-[(2-[3Z-hexenyl]-cyclopropyl)- methyl]- 1186

Propanamide, N-ethenyl-N-[(2-[3Z- hexenyl]-cyclopropyl)-methyl]- 1187

Propanamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-(2- propenyl)- 1188

Propanamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1189

Propanamide, N-butyl-N-[(2-[3Z- hexenyl]-cyclopropyl)-methyl]- 1190

Propanamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-(2- methylpropyl)- 1191

Acetamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-methyl- 1192

Acetamide, N-ethyl-N-[(2-[3Z- hexenyl]-cyclopropyl)-methyl]- 1193

Acetamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-propyl- 1194

Acetamide, N-(1-methylethyl)-N-[(2- [3Z-hexenyl]-cyclopropyl)-methyl]- 1195

Acetamide, N-(1,1-dimethylethyl)-N- [(2-[3Z-hexenyl]-cyclopropyl)- methyl]- 1196

Acetamide, N-ethenyl-N-[(2-[3Z- hexenyl]-cyclopropyl)-methyl]- 1197

Acetamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-(2- propenyl)- 1198

Acetamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1199

Acetamide, N-butyl-N-[(2-[3Z- hexenyl]-cyclopropyl)-methyl]- 1200

Acetamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-(2- methylpropyl)- 1201

Acetamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-methyl- 1202

Acetamide, N-ethyl-N-[(2-[3Z- hexenyl]-cyclopropyl)-methyl]- 1203

Acetamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-propyl- 1204

Acetamide, N-(1-methylethyl)-N-[(2- [3Z-hexenyl]-cyclopropyl)-methyl]- 1205

Acetamide, N-(1,1-dimethylethyl)-N- [(2-[3Z-hexenyl]-cyclopropyl)- methyl]- 1206

Acetamide, N-ethenyl-N-[(2-[3Z- hexenyl]-cyclopropyl)-methyl]- 1207

Acetamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N-(2- propenyl)- 1208

Acetamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl]-N- (cyclopropylmethyl)- 1209

Acetamide, N-butyl-N-[(2-[3Z- hexenyl]-cyclopropyl)-methyl]- 1210

Acetamide, N-[(2-[3Z-hexenyl]- cyclopropyl)-methyl ]-N-(2- methylpropyl)- 1211

2-butenamide, N-[(2E)-3,7-dimethyl- 2,6-octadienyl]-2-methyl-(2E)- 1212

2-butenamide, N-[(2Z)-3,7-dimethyl- 2,6-octadienyl]-2-methyl-(2E)- 1213

2-butenamide, N-[[2-methyl-2-(4- methyl-3- pentenyl)cyclopropyl]methyl]- 1214

Acetamide, N-[[2-methyl-2-(4- methyl-3- pentenyl)cyclopropyl]methyl]- 1215

Propanamide, N-[[2-methyl-2-(4- methyl-3- pentenyl)cyclopropyl]methyl]- 1216

Propanamide, N-[[2-methyl-2-(4- methyl-3- pentenyl)cyclopropyl]methyl]-2- methyl- 1217

2-methyl-2-(4-methyl-3- pentenyl)Cyclopropanecarboxamide, N-cyclopropyl- 1218

2-methyl-2-(4-methyl-3-pentenyl) Cyclopropanecarboxamide, N-2- propenyl- 1219

2-methyl-2-(4-methyl-3-pentenyl) Cyclopropanecarboxamide, N-2- methylpropanyl- 1220

2-methyl-2-(4-methyl-3-pentenyl)- Cyclopropanecarboxamide, N-methyl- 1221

2-methyl-2-(4-methyl-3-pentenyl)- Cyclopropanecarboxamide, N-ethyl- 1222

2-methyl-2-(4-methyl-3-pentenyl) Cyclopropanecarboxamide, N-1- methylethyl- 1223

2-methyl-2-(4-methyl-3-pentenyl) Cyclopropanecarboxamide, N- cyclopropyl- 1224

2-methyl-2-(4-methyl-3-pentenyl) Cyclopropanecarboxamide, N,N- dimethyl-

We have surprisingly found the literature has not previously reported dienalkylamides, alkenylamides, or cyclopropylic amides as having or enhancing umami flavor. In addition, closely structurally related compounds such as dienals and unsaturated acids, are not specifically reported to possess umami character when tasted in isolation. In addition the ability to provide an enhanced saltiness for the product without increasing sodium level is not disclosed or suggested by the prior art. The salt enhancing properties of the compounds of the present invention are important because it allows flavorists to provide the desired salty taste profile in foods and beverages without actually having higher salt levels in the food. Therefore the consumer can have both the taste profile that they desire while without having the adverse health effects associated with increased salt levels such as hypertension.

As used herein olfactory effective amount is understood to mean the amount of compound in flavor compositions the individual component will contribute to its particular olfactory characteristics, but the flavor, taste and aroma effect on the overall composition will be the sum of the effects of each of the flavor ingredients. As used herein taste effects include salt, sweet and umami effects. Thus the compounds of the invention can be used to alter the taste characteristics of the flavor composition by modifying the taste reaction contributed by another ingredient in the composition. The amount will vary depending on many factors including other ingredients, their relative amounts and the effect that is desired.

The level of cyclopropylic amides, alkenylamides and dienalkylamides used in products is greater than 50 parts per billion, generally provided at a level of from about 0.01 parts per million to about 50 parts per million in the finished product, more preferably from about 0.1 parts per million to about 20 parts per million by weight, and in preferred embodiments from about 0.5 to about 5 parts per million.

The usage level of cyclopropylic amides, alkenylamides, and dienalkylamides varies depending on the product in which the dienalkylamides are employed. For example, alcoholic beverages the usage level is from about 0.1 to about 5 parts per million, preferably from about 0.5 to about 3 and most preferably from about 1 to about 2 parts per million by weight. Non-alcoholic beverages are flavored at levels of from about 0.05 parts per million to about 5 parts per million, preferably from about 0.1 parts per billion to about 2 parts per million and in highly preferred situations of from about 0.7 to about 1 parts per billion. Other products such as snack foods, candy and gum products can be advantageously flavored using compounds of the present invention at levels described above.

Among the preferred compounds of the present invention are: 2-butenamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-, (2E)-2-butenamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-, (2E)-2-butenamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-3-methyl-2-butenamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-3-methyl-2-butenamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-2-methyl-(2E)-2-butenamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-2-methyl-(2E)-Cyclopropanecarboxamide, N-[(2Z,6Z)_(t)-2,6-nonadienyl]-Cyclopropanecarboxamide, N-[(2E,6Z)-2,6-nonadienyl]-Cyclopropanecarboxamide, N-[(2E)-3-(3-cyclohexen-1-yl)-2-propenyl]-Cyclopropanecarboxamide, N-[(2E,6Z)-2,6-dodecadienyl]-Cyclopropanecarboxamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-Cyclopropanecarboxamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-Propanamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-2-methyl-Propanamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-2-methyl-Acetamide, N-[(2Z,6Z)-2,6-nonadienyl]-Acetamide, N-[(2E,6Z)-2,6-nonadienyl]-Acetamide, N-[(2Z,6Z)-2-methyl-2,6-nonadienyl]-Acetamide, N-[(2Z,6Z)-2-methyl-2,6-nonadienyl]-Cyclopropanecarboxamide, N-[[2-methyl-2-(4-methyl-3-pentenyl)cyclopropyl]methyl]-Acetamide, N-[[2-methyl-2-(4-methyl-3-pentenyl)cyclopropyl]methyl]-Cyclopropanecarboxamide, N-methyl-N-[(2E,6Z)-2,6-nonadienyl]-Cyclopropanecarboxamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-N-methyl-Cyclopropanecarboxamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-N-ethyl-Propanamide, N-[(2E,6Z)-2,6-nonadienyl]-N-cyclopropylmethyl-.

The present invention also provides a method for enhancing or modifying the salt flavor of a food through the incorporation of an organoleptically acceptable level of the compounds described herein. The compounds can be used individually or in combination with other salt enhancing compounds of the present invention. In addition, the salt enhancing materials of the present invention can be used in combination with other salt enhancing compositions known in the art, including those materials listed in co-pending applications U.S. Ser. No. 10/919,631 filed on Aug. 17, 2004; U.S. Ser. No. 10/861,751 filed on Jun. 4, 2004; and U.S. Ser. No. 10/783,652 filed Feb. 20, 2004; and also include cetylpyridium chloride, bretylium tosylate, various polypeptides, mixtures of calcium salts of ascorbic acid, sodium chloride and potassium chloride, as described in various U.S. Pat. Nos. 4,997,672; 5,288,510; 6,541,050 and U.S. Patent Application 2003/0091721.

The salt taste enhancing compounds of the present invention may be employed to enhance the perceived salt taste of any salts used in food or beverage products. The preferred salt taste to be enhanced by the compounds of the present invention is that of sodium chloride, primarily because of the discovery that ingestion of large amounts of sodium may have adverse effects on humans and the resultant desirability of reducing salt content while retaining salt taste.

In addition, the compounds of the present invention may also be employed to enhance the perceived salt taste of known salty tasting compounds which may be used as salt substitutes, including potassium chloride and ribonucleotides. Suitable compounds also include cationic amino acids and low molecular weight dipeptides. Specific examples of these compounds are arginine hydrochloride, arginine ammonium chloride, lysine hydrochloride and lysine-ornithine hydrochloride. These compounds exhibit a salty taste but are typically useful only at low concentrations since they exhibit a bitter flavor at higher concentrations. Thus, it is feasible to reduce the sodium chloride content of a food or beverage product by first formulating a food or beverage with less sodium chloride than is necessary to achieve a desired salt taste and then adding to said food or beverage the compounds of the present invention in an amount sufficient to potentiate the salt taste of said salted food or beverage to reach said desired taste. In addition, the sodium chloride content may be further reduced by substituting a salty-tasting cationic amino acid, a low molecular weight dipeptide or mixtures thereof for at least a portion of the salt.

In a preferred embodiment of the present invention we have found the compound of the present invention are materials used in combination with each other or other salt enhancing materials in weight ratios of from about 1:10 to about 10:1, typically from about 1:3 to about 3:1; more preferably from about 1:1 on a weight basis.

In a highly preferred embodiment we have discovered that the compounds of the present invention when used in combination with the compounds disclosed in co-pending application U.S. Ser. No. 10/783,652 filed Feb. 20, 2004. The preferred compounds disclosed in this application include but are not limited to: N,N,3,7-Tetramethylocta-2,6-dienamide,(2E)-2-propenamide, 3-(3-cyclohexen-1-yl)-N-ethyl-,(2E)-3,7-dimethyl-2,6-octadienamide, N-ethyl-,(2E)-2,6-nonadienamide, N,N-dimethyl-, (2E,6Z)-2,6-nonadienamide, N-cyclopropyl, 2-methyl-, (2E,6Z)-2,6-dodecadienamide, N-ethyl-, (2E,6Z)-2,6-nonadienamide, N-cyclopropyl-, (2E,6Z)-2,6-nonadienamide, N-ethyl-, (2E,6Z)-.

The mixtures of the compounds range from about 1:10 to 10:1 weight percent, preferably from about 1:5 to about 5:1 weight percent, most preferably in a 1:2 to a 2:1 weight ratio of the compounds.

Combinations that have been found to provide high levels of salt and umami enhancing effects to products are compounds of the present invention: 2-butenamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-, (2E)-2-butenamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-, (2E)-2-butenamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-3-methyl-2-butenamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-3-methyl-2-butenamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-2-methyl-(2E)-2-butenamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-2-methyl-(2E)-Cyclopropanecarboxamide, N-[(2Z,6Z)_(t)-2,6-nonadienyl]-Cyclopropanecarboxamide, N-[(2E,6Z)-2,6-nonadienyl]-Cyclopropanecarboxamide, N-[(2E)-3-(3-cyclohexen-1-yl)-2-propenyl]-Cyclopropanecarboxamide, N-[(2E,6Z)-2,6-dodecadienyl]-Cyclopropanecarboxamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-Cyclopropanecarboxamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-Propanamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-2-methyl-Propanamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-2-methyl-Acetamide, N-[(2Z,6Z)-2,6-nonadienyl]-Acetamide, N-[(2E,6Z)-2,6-nonadienyl]-Acetamide, N-[(2Z,6Z)-2-methyl-2,6-nonadienyl]-Acetamide, N-[(2Z,6Z)-2-methyl-2,6-nonadienyl]-Cyclopropanecarboxamide, N-[[2-methyl-2-(4-methyl-3-pentenyl)cyclopropyl]methyl]-Acetamide, N-[[2-methyl-2-(4-methyl-3-pentenyl)cyclopropyl]methyl]-Cyclopropanecarboxamide, N-methyl-N-[(2E,6Z)-2,6-nonadienyl]-Cyclopropanecarboxamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-N-methyl-Cyclopropanecarboxamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-N-ethyl-Propanamide, N-[(2E,6Z)-2,6-nonadienyl]-N-cyclopropylmethyl-N,N,3,7-Tetramethylocta-2,6-dienamide,(2E)-2-propenamide, 3-(3-cyclohexen-1-yl)-N-ethyl-,(2E)-3,7-dimethyl-2,6-octadienamide, N-ethyl-,(2E)-2,6-nonadienamide, N,N-dimethyl-, (2E,6Z)-2,6-nonadienamide, N-cyclopropyl, 2-methyl-, (2E,6Z)-2,6-dodecadienamide, N-ethyl-, (2E,6Z)-2,6-nonadienamide, N-cyclopropyl-, (2E,6Z)-2,6-nonadienamide, N-ethyl-, (2E,6Z)-.

The highly preferred weight ratios of these mixtures is from about 2:1 to about 1:2 on a weight basis. Most highly preferred combination is the mixture of Cyclopropanecarboxamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]- with 2,6-nonadienamide, N-cyclopropyl-, (2E,6Z)- and 2,6-nonadienamide, N-ethyl-, (2E,6Z)- in the ratio about 2:1:1 by weight, with a total use level of 8 ppm. For purpose of illustration that would be a usage level of about 4, 2 and 2 parts per million respectively by weight in a product such as a foodstuff.

The term “foodstuff” as used herein includes both solid and liquid ingestible materials for man or animals, which materials usually do, but need not, have nutritional value. Thus, foodstuffs include food products, such as, meats, gravies, soups, convenience foods, malt, alcoholic and other beverages, milk and dairy products, seafood, including fish, crustaceans, mollusks and the like, candies, vegetables, cereals, soft drinks, snacks, dog and cat foods, other veterinary products and the like.

When the compounds of this invention are used in a flavoring composition, they can be combined with conventional flavoring materials or adjuvants. Such co-ingredients or flavor adjuvants are well known in the art for such use and have been extensively described in the literature. Requirements of such adjuvant materials are: (1) that they be non-reactive with the compounds of our invention; (2) that they be organoleptically compatible with the compounds of our invention whereby the flavor of the ultimate consumable material to which the compounds are added is not detrimentally affected by the use of the adjuvant; and (3) that they be ingestible acceptable and thus nontoxic or otherwise non-deleterious. Apart from these requirements, conventional materials can be used and broadly include other flavor materials, vehicles, stabilizers, thickeners, surface active agents, conditioners and flavor intensifiers.

Such conventional flavoring materials include saturated fatty acids, unsaturated fatty acids and amino acids; alcohols including primary and secondary alcohols, esters, carbonyl compounds including ketones, other than the dienalkylamides of our invention and aldehydes; lactones; other cyclic organic materials including benzene derivatives, acyclic compounds, heterocyclics such as furans, pyridines, pyrazines and the like; sulfur-containing compounds including thiols, sulfides, disulfides and the like; proteins; lipids, carbohydrates; so-called flavor potentiators such as monosodium glutamate; magnesium glutamate, calcium glutamate, guanylates and inosinates; natural flavoring materials such as hydrolyzates, cocoa, vanilla and caramel; essential oils and extracts such as anise oil, clove oil and the like and artificial flavoring materials such as vanillin, ethyl vanillin and the like.

Specific preferred flavor adjuvants include but are not limited to the following: anise oil; ethyl-2-methyl butyrate; vanillin; cis-3-heptenol; cis-3-hexenol; trans-2-heptenal; butyl valerate; 2,3-diethyl pyrazine; methyl cyclo-pentenolone; benzaldehyde; valerian oil; 3,4-dimethoxy-phenol; amyl acetate; amyl cinnamate; y-butyryl lactone; furfural; trimethylpyrazine; phenyl acetic acid; isovaleraldehyde; ethyl maltol; ethyl vanillin; ethyl valerate; ethyl butyrate; cocoa extract; coffee extract; peppermint oil; spearmint oil; clove oil; anethol; cardamom oil; wintergreen oil; cinnamic aldehyde; ethyl-2-methyl valerate; y-hexenyl lactone; 2,4-decadienal; 2,4-heptadienal; methyl thiazole alcohol (4-methyl-5-p-hydroxyethyl thiazole); 2-methyl butanethiol; 4-mercapto-2-butanone; 3-mercapto-2-pentanone; 1-mercapto-2-propane; benzaldehyde; furfural; furfuryl alcohol; 2-mercapto propionic acid; alkyl pyrazine; methyl pyrazine; 2-ethyl-3-methylpyrazine; tetramethylpyrazine; polysulfides; dipropyl disulfide; methyl benzyl disulfide; alkyl thiophene; 2,3-dimethyl thiophene; 5-methyl furfural; acetyl furan; 2,4-decadienal; guiacol; phenyl acetaldehyde; β-decalactone; d-limonene; acetoin; amyl acetate; maltol; ethyl butyrate; levulinic acid; piperonal; ethyl acetate; n-octanal; n-pentanal; n-hexanal; diacetyl; monosodium glutamate; mono-potassium glutamate; sulfur-containing amino acids, e.g., cysteine; hydrolyzed vegetable protein; 2-methylfuran-3-thiol; 2-methyldihydrofuran-3-thiol; 2,5-dimethylfuran-3-thiol; hydrolyzed fish protein; tetramethylpyrazine; propylpropenyl disulfide; propylpropenyl trisulfide; diallyl disulfide; diallyl trisulfide; dipropenyl disulfide; dipropenyl trisulfide; 4-methyl-2-[(methylthio)-ethyl]-1,3-dithiolane; 4,5-dimethyl-2-(methylthiomethyl)-1,3-dithiolne; and 4-methyl-2-(methylthiomethyl)-1,3-dithiolane. These and other flavor ingredients are provided in U.S. Pat. Nos. 6,110,520 and 6,333,180.

The cyclopropylic amides, alkenylamides, and dienalkylamides of our invention or compositions incorporating them, as mentioned above, can be combined with one or more vehicles or carriers for adding them to the particular product. Vehicles can be edible or otherwise suitable materials such as ethyl alcohol, propylene glycol, water and the like, as described above. Carriers include materials such as gum arabic, carrageenan, xanthan gum, guar gum and the like.

Cyclopropylic amides, alkenylamides, and dienalkylamides prepared according to our invention can be incorporated with the carriers by conventional means such as spray-drying, extrusion, drum-drying and the like. Such carriers can also include materials for coacervating the dienalkylamides of our invention to provide encapsulated products, as set forth above. When the carrier is an emulsion, the flavoring composition can also contain emulsifiers such as mono- and diglycerides or fatty acids and the like. With these carriers or vehicles, the desired physical form of the compositions can be prepared.

The quantity of cyclopropylic amides, alkenylamides, and dienalkylamides utilized should be sufficient to impart the desired flavor characteristic to the product, but on the other hand, the use of an excessive amount of the compounds is not only wasteful and uneconomical, but in some instances, too large a quantity may unbalance the flavor or other organoleptic properties of the product consumed. The quantity used will vary depending upon the ultimate foodstuff; the amount and type of flavor initially present in the foodstuff; the further process or treatment steps to which the foodstuff will be subjected; regional and other preference factors; the type of storage, if any, to which the product will be subjected; and the preconsumption treatment such as baking, frying and so on, given to the product by the ultimate consumer. Accordingly, the terminology “organoleptically effective amount” and “sufficient amount” is understood in the context of the present invention to be quantitatively adequate to alter the flavor of the foodstuff.

With reference to the novel compounds of our invention, the synthesis is effected by means of the reaction of acid anhydride with amine, added either directly or in solution, according to the general scheme:

where R¹, R², R³, R⁴, R⁵ and R⁶ have the meaning set forth in formula I, and structures 1 and 2 set forth above.

The synthesis of amine follows a literature procedure [The Journal of organic Chemistry 1989, 54, 3292-3303]. The acid anhydride is dissolved in hexanes to which amine is added in 0.9 to 1.0 equivalent at temperatures ranging 0° C. to room temperature, most preferably from 10° C. to 20° C. The resulting solution is aged for about 1-3 hours at room temperature.

The reaction can be quenched with aqueous sodium chloride, hydrogen chloride or sodium hydroxide depending upon the need to remove residual acid or amine. The mixture is extracted into ethereal solvent, washed to neutrality and solvent removed.

The crude product is purified by distillation or recrystallization depending on the physical properties. The reaction occurs in 35-70% mole yield based on amine.

In the case when acid anhydride is not readily available, the synthesis is effected by means of the reaction of acid with ethyl chloroformate in the presence of triethylamine and further reaction of the intermediate with amine, added either directly or in solution, according to the general scheme:

where R¹, R², R³, R⁴, R⁵ and R⁶ have the meaning set forth in formula I, and structures 1 and 2 set forth above.

The acid is dissolved in dichloromethane to which ethyl chloroformate is added in 1.0 to 2.0 equivalents at temperatures ranging from 0° C. to room temperature, most preferably from 10° C. to 20° C. The resulting solution is cooled to −10° C. to −30° C., and triethylamine is added in 1.0 to 2.0 equivalents such that the temperature range is below 0° C. and the mixture aged for 1 hour.

The mixture is filtered, and the filtrate cooled to 0° C. The amine is added in 1.0 to 7.0 equivalents either neat or as a solution in a suitable solvent, the reaction is then aged for about 1-3 hours at room temperature.

The reaction can be quenched with aqueous sodium chloride, hydrogen chloride or sodium hydroxide depending upon the need to remove residual acid or amine. The mixture is extracted into ethereal solvent or dichloromethane, washed to neutrality and solvent removed.

The crude product is purified by distillation or re-crystallization depending on the physical properties.

The reaction occurs in 35-75% mole yield based on acid.

The dienalkylamides of the present invention can be admixed with other flavoring agents and incorporated into foodstuffs and other products using techniques well known to those with ordinary skill in the art. Most commonly the dienalkylamides are simply admixed using the desired ingredients within the proportions stated.

In the preparation of the amides of structure 2 the synthesis of the starting amine can be effected by means of the reaction cyclopropylalkenamines which are formed through standard reduction processes of nitrites using techniques well known to those with ordinary skill in the art. Such nitriles are disclosed in commonly assigned U.S. application Ser. No. 11/154,399 filed Jun. 17, 2005. Specifically, cyclopropanecarbonitriles such as 2-methyl-2-(4-methylpent-3-en-1-yl)-cyclopropanecarbonitrile which may be prepared from the corresponding alkenenitriles, via Corey's cyclopropanation reaction from the corresponding alkenenitriles commercially available from International Flavors & Fragrances Inc., New York, N.Y. The corresponding alkenenitrile is 3,7-dimethyl-octa-2,6-dienenitrile, which is also known under the tradename Citralva.

Those with skill in the art will recognize that the compounds of the present invention have a number of chiral centers, thereby providing several isomers of the claimed compounds. It is intended herein that the compounds described herein include isomeric mixtures of such compounds, as well as those isomers that may be separated using techniques known to those having skill in the art. Suitable techniques include chromatography such as HPLC, and particularly gel chromatography and solid phase microextraction (“SPME”).

The following are provided as specific embodiments of the present invention. Other modifications of this invention will be readily apparent to those skilled in the art, without departing from the scope of this invention. As used herein, in both the specification and following examples, all percentages are understood to be weight percent unless noted to the contrary.

All U.S. Patents and U.S. Patent Applications cited herein are incorporated by reference as if set forth in their entirety. Upon review of the foregoing, numerous adaptations, modifications, and alterations will occur to the reviewer. These will all be, however, within the spirit of the present invention. Accordingly, reference should be made to the appended claims in order to ascertain the true scope of the present invention.

EXAMPLE 1 Preparation of Materials of the Present Invention

The following reaction sequence was used to prepare the specific compounds described by the NMR data set forth below:

where R¹, R², R³, R⁴, R⁵ and R⁶ have the meaning set forth in formula I, and structures 1 and 2 set forth above.

The acid anhydride was dissolved in hexanes to which amine was added in 0.9 to 1.0 equivalent at temperatures ranging from 0° C. to room temperature, most preferably from 10° C. to 20° C. The resulting solution was aged for about 1-3 hours at room temperature.

The reaction was quenched with aqueous sodium chloride, hydrogen chloride or sodium hydroxide depending upon the need to remove residual acid or amine. The mixture was extracted into ethereal solvent, washed to neutrality and solvent removed.

The crude product was purified by distillation or recrystallization depending on the physical properties.

The amides were synthesized according to the general scheme above with the following specific examples. Equivalents set out are mole equivalents based on starting amine, yields were distilled chemical yields based on starting amine.

Butanamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-

Butyric anhydride 1.1eq, 3,7-dimethylocta-2E,6-dienylamine 1 eq, quenched with 10% sodium hydroxide, yield=35%.

¹H NMR 0.95 ppm (3H, t, J=7.34 Hz), 1.60 ppm (3H, s), 1.62-1.71 ppm (2H, m), 1.67 ppm (3H, s), 1.68 ppm (3H, s), 2.01 ppm (2H, m), 2.08 ppm (2H, m), 2.15 ppm (2H, m), 3.85 ppm (2H, m), 5.08 ppm (1H, m), 5.19 ppm (1H, m), 5.44 ppm (1H, br. s).

2-butenamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-(2E)

Crotonic anhydride 1.1eq, 3,7-dimethylocta-2E,6-dienylamine 1 eq, quenched with 10% sodium hydroxide, yield=70%.

¹H NMR 1.60 ppm (3H, s), 1.68 ppm (6H, m), 1.84-1.91 ppm (3H, m), 1.94-2.09 ppm (4H, m), 3.84 ppm (1H, m), 3.91 ppm (1H, m), 5.08 ppm (1H, m), 5.21 ppm (1H, m), 5.34 ppm (1H, br. s), 5.79 ppm (1H, d, J=15.15 Hz), 6.84 ppm (1H, m).

Propanamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-2-methyl-

2-Methylpropionic anhydride 1.1eq, 3,7-dimethylocta-2E,6-dienylamine 1 eq, quenched with 10% sodium hydroxide, yield=58%.

¹H NMR 1.17 ppm (d, 6H, J=6.5 Hz), 1.63 ppm (3H, s), 1.69 ppm (3H, s), 1.71 ppm (3H, s), 2.04 ppm (2H, m), 2.08 ppm (2H, m), 2.82 (1H, m), 3.87 ppm (2H, m), 5.10 ppm (1H, m), 5.26 ppm (1H, m), 5.56 ppm (1H, br. s).

Propanamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-

Propionic anhydride 1.1eq, 3,7-dimethylocta-2Z,6-dienylamine 1 eq, quenched with 10% sodium hydroxide, yield=76%.

¹H NMR 1.15 ppm (m, 3H), 1.60 ppm (s, 3H), 1.69 ppm (s, 3H), 1.72 ppm (s, 3H), 1.98-2.28 ppm (m, 6H), 3.31-3.37 ppm (m, ˜25% of 2H), 3.81-3.83 ppm (m, ˜75% of 2H), 5.09 ppm (s, 1H), 5.20 ppm (m, 1H), 5.59 ppm (br. s, 1H).

Acetamide, N-[(2E,6Z)-nonadienyl]-

Procedure: 1.0 equiv nonyl-2,6-dienylamine, 1.1 equiv acetic anhydride, quenched with 10% sodium hydroxide, 60% yield

¹H NMR (500 MHz, CDCl₃) 5.65-5.60 (m, 1H), 5.53-5.37 (m, 3H), 5.33-5.28 (m, 1H), 3.82 (t, J=5.7 Hz, 2H), 2.17-2.06 (m, 4H), 2.05-2.02 (m, 2H), 1.99 (s, 3H), 0.96 (t, J=7.53 Hz, 3H).

Propanamide, N-[(2E,6Z)-nonadienyl]-

Procedure: 1.0 equiv nonyl-2,6-dienylamine, 1.1 equiv proponoic anhydride, quenched with 10% sodium hydroxide, 63% yield.

¹H NMR (500 MHz, CDCl₃) 5.86 (bs, 1H), 5.63-5.30 (m, 4H), 3.81 (s, 2H), 2.23-2.19 (q, J=7.4 Hz, 2H), 2.09-2.01 (m, 6H), 1.16 (t, J=7.5 Hz, 3H), 0.96 (t, J=7.4 Hz, 3H).

Acetamide, N-[2,6-nonadienyl]-2-methyl-(6Z)-

Procedure: 1.0 equiv 2-methyl-nonyl-2,6-dienylamine, 1.1 equiv acetic anhydride, quenched with 10% sodium hydroxide, 53% yield

¹H NMR (500 MHz, CDCl₃) 5.52-5.30 (m, 4H), 3.85 (d, J=5.43 Hz, 0.6H), 3.78 (d, J=5.77 Hz, 1.4H), 2.13-2.01 (m, 6H), 2.00 (s, 0.9H), 1.98 (s, 2.1H), 1.72 (s, 0.9H), 1.62 (s, 2.1H), 0.96 (t, J=7.53 Hz, 3H).

Acetamide, N-[(2E)-3-(2,4-dimethyl-3-cyclohexen-1-yl)-2-propenyl]-

Procedure: 1.0 equiv 3-(2,4-dimethyl)-cyclohex-3-enyl)-allylamine, 1.1 equiv acetic anhydride, quenched with 10% sodium hydroxide, 67% yield

¹H NMR (500 MHz, CDCl₃) δ 5.75 (bs, 1H), 5.66-5.28 (m, 2H), 5.35-5.25 (d, 0.5H), 5.18 (s, 0.5H), 3.81-3.82 (d, J=5.27 Hz, 2H), 1.98 (s, 3H), 2.05-1.95 (m, 1H), 1.94-1.77 (m, 2H), 1.75-1.57 (m, 2H), 1.63 (s, 3H), 1.54-1.37 (m, 1H), 0.92-0.86 (m, 2.5H), 0.82-0.72 (t, J=7.2 Hz, 0.5H).

Acetamide, N-[(2E)-2-methyl-3-phenyl-2-propenyl]-

Procedure: 1.0 equiv 2-methyl-3-phenyl-allylamine, 1.1 acetic anhydride, quenched with 10% sodium hydroxide, 67% yield

¹H NMR (500 MHz, CDCl₃) δ 7.32-7.16 (m, 5H), 6.45 (s, 0.8H), 6.38 (s, 0.2H), 5.81 (s, 0.2H), 5.58 (s, 0.8H), 4.06 (d, J=5.61 Hz, 1.6H), 3.96 (d, J=5.97 Hz, 0.4H), 2.04 (s, 0.9H), 1.96 (s, 2.1H), 1.90 (s, 2.3H), 1.86 (s, 0.7H).

Propanamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-2-methyl-

Isobutyric anhydride 1.1eq, 3,7-dimethylocta-2Z,6-dienylamine 1 eq, quenched with 10% sodium hydroxide, yield=80%.

¹H NMR 1.15 ppm (d, 6H, J=6.8 Hz, of d, J=2.4 Hz), 1.60-1.73 ppm (m, 9H), 1.98-2.24 ppm (m, 4H), 2.27-2.35 ppm (m, 1H), 3.83 ppm (m, 2H), 5.09 ppm (m, 1H), 5.16-5.28 ppm (m, 1H), 5.46 ppm (br. s, 1H).

EXAMPLE 2 Preparation of Materials of the Present Invention

The following reaction sequence was used to prepare the specific compounds described by the NMR data set forth below:

The acid was dissolved in dichloromethane to which ethyl chloroformate was added in 1.0 to 2.0 equivalents at temperatures ranging from 0° C. to room temperature, most preferably from 10° C. to 20° C. The resulting solution was cooled to −10° C. to −30° C., and triethylamine is added in 1.0 to 2.0 equivalents such that the temperature range was below 0° C. and the mixture aged for 1 hour.

The mixture was filtered, and the filtrate cooled to 0° C. The amine was added in 1.0 to 7.0 equivalents either neat or as a solution in THF and the reaction was aged for about 1-3 hours at room temperature.

The reaction was quenched with aqueous sodium chloride, hydrogen chloride or sodium hydroxide depending upon the need to remove residual acid or amine. The mixture was extracted into ethereal solvent or dichloromethane, washed to neutrality and solvent removed.

The crude product was purified by distillation or recrystallization depending on the physical properties.

The amides were synthesized according to the general scheme above with the following specific examples. Equivalents set out are mole equivalents based on starting acid, yields were distilled chemical yields based on starting acid.

In some of the following examples acid chloride is used in place of carboxylic acid and ethyl chloroformate.

2,6-nonadienamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-, (2E,6Z)-

2E,6Z-Nonadienoic acid 1.0eq, ethyl chloroformate 1.5eq, triethylamine 1.5eq, 3,7-dimethylocta-2E,6-dienylamine 1.6eq, quenched with 10% sodium chloride solution, yield=50%.

¹H NMR 0.95 ppm(t, 3H, J=7.53 Hz), 1.60 ppm (s, 3H), 1.68 ppm (s, 6H), 1.96-2.13 ppm (m, 6H), 2.17-2.22 ppm (m, 4H), 3.91 ppm (t, 2H, J=6.07 Hz), 5.06-5.09 ppm (m, 1H), 5.22 ppm (t, 1H, J=6.98 Hz), 5.28-5.33 ppm (m, 1H), 5.37-5.43 ppm (m, 1H), 5.58 ppm (br. s, 1H), 5.79 ppm (d, 1H, J=15.33 Hz), 6.82 ppm (d, 1H, J=15.25 Hz, of t, J=6.59 Hz).

Propanamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-2,2-dimethyl-

Trimethylacetic acid 1.0 eq, ethyl chloroformate 1.5eq, triethylamine 1.5eq, 3,7-dimethylocta-2E,6-dienylamine 1.6eq, quenched with 10% sodium chloride solution, yield=41%.

¹H NMR 1.20 ppm (2s, 9H), 1.60 ppm (s, 3H), 1.67 ppm (s, 3H), 1.68 ppm (s, 3H), 1.98-2.10 ppm (m, 4H), 3.82-3.84 ppm (m, 2H), 5.07-5.09 ppm (m, 1H), 5.17-5.20 ppm (m, 1H), 5.53 ppm (br. s, 1H).

2-butenamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-3-methyl-

3,3-Dimethylacrylic acid 1.0eq, ethyl chloroformate 1.5eq, triethylamine 1.5eq, 3,7-dimethylocta-2E,6-dienylamine 1.6eq, quenched with 10% sodium chloride solution, yield=16%.

¹H NMR 1.60 ppm (s, 3H), 1.67 ppm (s, 3H), 1.68 ppm (s, 3H), 1.83 ppm (s, 3H), 1.95-2.02 ppm (m, 2H), 2.06-2.13 ppm (m, 2H), 2.15 ppm (s, 3H), 3.85-3.89 ppm (m, 2H), 5.07-5.09 ppm (m, 1H), 5.20-5.22 ppm (m, 1H), 5.42 ppm (br. s, 1H), 5.56 ppm (s, 1H).

2-butenamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-2-methyl-(2E)

2-Methyl-2E-butenoic acid 1.0eq, ethyl chloroformate 1.5eq, triethylamine 1.5eq, 3,7-dimethylocta-2E,6-dienylamine 1.6eq, quenched with 10% sodium chloride solution, yield=31%.

¹H NMR 1.60 ppm (s, 3H), 1.68-1.71 ppm (2s, 6H), 1.74-1.75 ppm (2s, 3H), 1.84 ppm (s, 3H), 1.96-2.03 ppm (m, 2H), 2.07-2.15 ppm (m, 2H), 3.89-3.91 ppm (m, 2H), 5.07-5.09 ppm (m, 1H), 5.21-5.24 ppm (m, 1H), 5.60 ppm (br. s, 1H), 6.40-6.42 ppm (m, 1H).

Butanamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-2-methyl-

2-Methylbutanoic acid 1.0eq, ethyl chloroformate 1.5eq, triethylamine 1.5eq, 3,7-dimethylocta-2E,6-dienylamine 1.6eq, quenched with 10% sodium chloride solution, yield=46%.

¹H NMR 0.89-0.92 ppm (m, 3H), 1.12-1.17 ppm (m, 3H), 1.39-1.45 ppm (m, 1H), 1.51-1.80 ppm (m, 1H), 1.60 ppm (s, 3H), 1.67 ppm (s, 3H), 1.68 ppm (s, 3H), 1.97-2.17 ppm (m, 5H), 3.86 ppm (s, 2H), 5.08 ppm (s, 1H), 5.18-5.21 ppm (m, 1H), 5.30-5.67 ppm (br. s, 1H).

Cyclopropanecarboxamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-

Cyclopropanecarboxic acid 1.0eq, ethyl chloroformate 1.5eq, triethylamine 1.5eq, 3,7-dimethylocta-2Z,6-dienylamine 1.6eq, quenched with 10% sodium chloride solution, yield=56%.

¹H NMR 0.70-0.71 ppm (m, 2H), 0.94-0.96 ppm (m, 2H), 1.30-1.34 ppm (m, 1H), 1.61-1.73 ppm (m, 9H), 1.98-2.28 ppm (m, 4H), 3.83-3.88 ppm (m, 2H), 5.10 ppm (m, 1H), 5.20-5.24 ppm (m, 1H), 5.72 ppm (br. s, 1H).

Cyclopropanecarboxamide, N-(3-methyl-2-butenyl)-

Cyclopropanecarboxic acid 1.0eq, ethyl chloroformate 1.5eq, triethylamine 1.5eq, 3-methyl-2-butenylamine 1.6eq, quenched with 10% sodium chloride solution, yield=17%.

¹H NMR 0.69-0.73 ppm (m, 2H), 0.95-0.98 ppm (m, 2H), 1.28-1.33 ppm (m, 1H), 1.68 ppm (s, 3H), 1.73 ppm (s, 3H), 3.85 ppm (t, 2H, J=6.1 Hz), 5.21 ppm (t, 1H, J=7.1 Hz), 5.50 ppm (br. s, 1H).

Cyclopropylcarboxamide, N-[2,6-dodecadienyl]-(2E,6Z)-

Procedure: 1.0 equiv dodecyl-2,6-dienylamine, 1.1 equiv cyclopropanecarbonyl chloride, 1.5 equiv triethylamine, quenched with water, 61% yield.

¹H NMR (500 MHz, CDCl₃) 5.65-5.61 (m, 2H), 5.50-5.46 (m, 1H), 5.40-5.33 (m, 2H), 3.84 (m, 2H), 2.11-2.07 (m, 4H), 2.03-1.99 (m, 2H), 1.35-1.26 (m, 7H), 0.99-0.96 (m, 2H), 0.89 (t, J=7.18 Hz, 3H), 0.74-0.71 (m, 2H).

Acetamide, N-[(2E)-3-(4-methyl-3-cyclohexen-1-yl)-2-butenyl]-

Procedure: 1.0 equiv 3-(4-methyl-cyclohex-3-enyl)-but-2-enylamine, 1.1 equiv acetyl chloride, 1.5 equiv triethylamine, quenched with water, 42% yield

¹H NMR (500 MHz, CDCl₃) δ 6.13 (bs, 1H), 5.38 (s, 1H), 5.23-5.16 (m, 1H), 3.87-3.79 (m, 2H), 2.16-2.02 (m, 2H), 1.97 (s, 3H), 2.01-1.95 (m, 1H), 1.92-1.77 (m, 1H), 1.74-1.68 (m, 1H), 1.66-1.60 (m, 6H), 1.59-1.25 (m, 2H).

Cyclopropylcarboxamide, N-[2,6-nonadienyl]-(2E,6Z)-

Procedure: 1.0 equiv nonyl-2,6-dienylamine, 1.1 equiv cyclopropanecarbonyl chloride, 1.5 equiv triethylamine, quenched with water, 63% yield.

¹H NMR (500 MHz, CDCl₃) 5.80-5.28 (m, 5H), 3.90 (d, J=6.06 Hz, 0.33H), 3.84 (t, J=5.65 Hz, 1.67H), 2.17-1.98 (m, 6H), 1.34-1.29 (m, 1H), 0.96 (t, J=7.5 Hz, 3H), 1.02-0.93 (m, 2.33H), 0.75-0.71 (m, 1.67H).

Cyclopropylcarboxamide, N-[2,6-nonadienyl]-2-methyl (2E,6Z)-

Procedure: 1.0 equiv 2-methyl-nonyl-2,6-dienylamine, 1.1 equiv cyclopropanecarbonyl chloride, 1.5 equiv triethylamine, quenched with water, 58% yield.

¹H NMR (500 MHz, CDCl₃) 5.52-5.30 (m, 4H), 3.91-3.80 (m, 2H), 2.13-1.95 (m, 6H), 1.73 (s, 1H), 1.63 (s, 2H), 1.38-1.28 (m, 1H), 0.96 (t, J=7.5 Hz, 3H), 1.00-0.94 (m, 1.5H), 0.93-0.84 (m, 1H), 0.75-0.71 (m, 1.5H).

Cyclopropanecarboxamide, N-[(2E)-3-(2,4-dimethyl-3-cyclohexen-1-yl)-2-propenyl]-

Procedure: 1.0 equiv 3-(2,4-dimethyl)-cyclohex-3-enyl)- allylamine, 1.1 equiv cyclopropanecarbonyl chloride, 1.5 equiv triethylamine, quenched with water, 65% yield.

¹H NMR (500 MHz, CDCl₃) δ 5.75 (bs, 1H), 5.66-5.44 (m, 2H), 5.35-5.28 (d, 0.5H), 5.19 (s, 0.5H), 3.90-3.79 (m, 2H), 2.05-1.81 (m, 3H), 1.65 (d, 3H), 1.72-1.57 (m, 1H), 1.57-1.41 (m, 1H), 1.40-1.18 (m, 2H), 0.97-0.95 (m, 2H), 0.92 (d, J=6.1 Hz, 1.8H), 0.89 (d, J=6.5 Hz, 1.2H), 0.73-0.70 (m, 2H).

Cyclopropanecarboxamide, N-[(2E)-2-methyl-3-phenyl-2-propenyl]-

Procedure: 1.0 equiv 2-methyl-3-phenyl-allylamine, 1.1 equiv cyclopropanecarbonyl chloride, 1.5 equiv triethylamine, quenched with water, 69% yield

¹H NMR (500 MHz, CDCl₃) δ 7.33 (dd, J=8.57, 7.33. Hz, 2H), 7.25 (d, J=8.57 Hz, 2H), 7.21 (t, J=7.33 Hz, 1H), 6.40 (s, 1H), 5.80 (bs, 1H), 4.00 (d, J=5.97 Hz, 2H), 1.87 (s, 3H), 1.41-1.38 (m, 1H), 1.02-1.00 (m, 2H), 0.78-0.75 (m, 2H).

Cyclopropanecarboxamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-

Cyclopropanecarboxylic acid 1 eq, ethyl chloroformate 1.5eq, triethylamine 1.5eq, 3,7-dimethylocta-2E,6-dienylamine 1.6eq, quenched with 10% sodium chloride solution, yield=36%.

0.71 ppm (2H, m), 0.96 ppm (2H, m), 1.33 ppm (1H, m), 1.60 ppm (3H, s), 1.67 ppm (3H, s), 1.69 ppm (3H, s), 2.01 ppm (2H, m), 2.08 ppm (2H, m), 3.87 ppm (2H, m), 5.08 ppm (1H, m), 5.21 ppm (1H, m), 5.61 ppm (1H, br. s).

EXAMPLE 3

Taste tests were conducted with various molecules. The following molecule (A) IS disclosed and claimed in this specification. Molecules (B) and (J) are disclosed and claimed as flavor materials in co-pending application U.S. Ser. No. 10/783,652 filed Feb. 20, 2004. These materials were used in the following taste examples.

-   (A) Cyclopropanecarboxamide,N-[(2E)-3,7-Dimethyl-2,6-Octadienyl] -   (B) (2E)-N,N,3,7-Tetramethylocta-2,6-dienamide -   (C) 2,6-Nonadienamide,N-2-Propenyl-,(2E,6Z) -   (D) N-isobutyl-(E2,Z6)-Nonadienamide -   (E) 2,6-Dodecadienamide,N-cyclopropyl-,(2E,6Z) -   (F) 2-butenamide,     N-ethyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-(2E) -   (G) 2,6-Octadienamide N-ethyl-3,7-dimethyl -   (H) Glycine N-[(2E,6Z)-1-oxo-2,6-nonadienyl]methyl ester -   (I) n-Cyclopropyl-(E2,Z6)-Nonadienamide -   (J) 2,6-Nonadienamide, N-ethyl-(2E,6Z)-

A trained consumer panel of about 16 flavorists, evaluated the above molecules in tasting solutions and were asked to rate the perception of salt and umami for each taste solution. The taste solutions presented to the panelists contained 0.3% by weight NaCl, 0.1% MSG and 0.015% Ribotides, a commercially available blend of disodium guanylate and disodium inosinate. The above molecules were added to the tasting solution at 1 and 4 parts per million.

The taste panel found the molecules of the invention increased the salt and umami perception in excess of 40%. This increase in the salty and umami taste of the base was higher than the increase seen when KCl was added to the base at levels of 0.12%, or when the total amount of salt, MSG and ribotides in the base were increased by 40%.

EXAMPLE 4

A trained panel of flavorists and scientists were given a series of paired taste samples containing by weight 0.3% NaCl, 0.1% MSG and 0.015% ribotides. For each member of the panel two samples were prepared. One sample given was the unaltered taste solution, the second sample was the sample one with the addition of one part per million of the above molecules. The panelists found the samples containing the molecules to have higher salt and umami character; the increase in salty and umami perception was increased by up to about 20%.

EXAMPLE 5

An expert panel of flavorists and food technologists were asked to blindly evaluate a series of reduced sodium beef broths containing between one and four ppm of the molecules of this invention set forth above. The panel found the broths to be significantly higher in saltiness and umami mouthfeel.

EXAMPLE 6

A commercially available rice side dish was prepared with and without the addition of compounds from this invention. The above described molecules were added at 3 ppm to the prepared rice mix. The rice mix was then prepared on the stove top according to the directions on the package. An expert panel of flavorists and food technologists were asked to rate the saltiness or the samples. The panel found that the rice samples with the addition of the molecules was significantly saltier than the unflavored reference.

The molecules of this invention were added to a commercially available noodle side dish at 2 ppm. A panel of flavorists and food technologists was presented the flavored and unflavored samples blind and asked to comment on the taste differences. The samples containing the molecules were uniformly rated as saltier than the unflavored samples.

EXAMPLE 7

The panel of flavorists and food technologists used in earlier examples were asked to evaluate a series of reduced sodium chicken broth versus a full sodium chicken broth. In this degree of difference testing, the panel was able to find a significant difference in the taste of chicken broth containing 10% less salt. The panel found the difference in the taste of the low salt sample to be pronounced when the salt was reduced by 15%.

Samples of lower salt chicken broth containing 800 parts per billion of the molecules of the invention provided above were given to this panel for evaluation. The panel could not perceive the difference between the full salt chicken broth and the chicken broth with 15% less salt containing the molecules set forth above. A sample of broth containing molecules of this invention with a 20% reduction in salt was not perceived as significantly different from the full salt broth.

EXAMPLE 8 Preparation of Materials of the Present Invention

The following reaction sequences were used to prepare the specific compounds described by the NMR data set forth below:

Cyclopropanecarboxyamide, N-methyl-N-[2,6-nonadienyl]-(E2,Z6)

To a reaction flask under nitrogen, NaH (2.0 g, 50 mmol) and 100 mL of toluene were charged. The reaction was heated to 80° C., and amide (10 g, 48 mmol) was fed over 25 minutes. The mixture was aged for 1 hour, then dimethylsulfide (DMS) (4.1 g, 33 mmol) was fed in to the reaction over 15 minutes. The reaction was allowed to age for 4 hours, and was then quenched with 85 g of 25% (wt/wt) NaOH solution. The reaction was aged at 80° C. for 1 hour, then the layers were separated and the organic layer was washed twice with warm water. The solvent was removed under reduced pressure. The product was purified by silica gel chromatography eluting with (0-50% EtOAc/hexanes) to give 6.3 g of product, 60% yield.

¹H NMR (500 MHz, CDCl₃) 5.59 (m, 1H), 5.50-5.36 (m, 2H), 5.30 (m, 1H), 4.01 (s, 1H), 3.94 (s, 1H), 3.07 (s, 1.5H), 2.91 (s, 1.5H), 2.12 (m, 4H), 2.03 (m, 2H), 1.71 (m, 1H), 0.96 (m, 2H), 0.96 (t, J=7.53 Hz, 3H), 0.73 (m, 2H).

Cyclopropanecarboxamide, N-[3,7-dimethyl-octa-2,6-dienyl]-N-methyl-(2E)

To a reaction flask under nitrogen, NaH (1.2 g, 29 mmol) and 50 mL of toluene were charged. The reaction was heated to 80° C., and amide (6.0 g, 27 mmol) dissolved in 25 mL of toluene was fed in over 30 minutes. The mixture was aged for 1 hour, then dimethylsulfide (2.4 g, 19 mmol) was fed in to the reaction over 5 minutes. The reaction was allowed to age for 4 hours, and was then quenched with 61 g of 25% (wt/wt) NaOH solution. The reaction was aged at 80° C. for 1 hour, then the layers were separated and the organic layer was washed twice with warm water. The solvent was removed under reduced pressure. The product was purified by kugelrohr distillation to give 4.2 g of product, 66% yield.

¹H NMR (500 MHz, CDCl₃) 5.21-5.11 (m, 1H), 5.08-5.07 (m, 1H), 4.08-4.02 (m, 1H), 3.88-3.85 (m, 1H), 3.07 (s, 1.5H), 2.91 (s, 1.5H), 2.10-2.00 (m, 4H), 1.73-1.68(m, 7H), 1.60 (m, 3H), 0.98-0.96 (m, 2H), 0.74-0.70 (m, 2H).

Cyclopropanecarboxamide, N-[3,7-dimethyl-octa-2,6-dienyl]-N-ethyl-(2E)

To a reaction flask under nitrogen, NaH (1.2 g, 29 mmol) and 50 mL of toluene were charged. The reaction was heated to 80° C., and amide (6.0 g, 27 mmol) dissolved in 25 mL of toluene was fed in over 30 minutes. The mixture was aged for 1 hour, then diethylsulfide (DES) (3.0 g, 19 mmol) was fed in to the reaction over 5 minutes. The reaction was allowed to age for 4-hours, and was then quenched with 61 g of 25% (wt/wt) NaOH solution. The reaction was aged at 80° C. for 1 hour, then the layers were separated and the organic layer was washed twice with warm water. The solvent was removed under reduced pressure. The product was purified by silica gel chromatography eluting with (0-50% EtOAc/hexanes) to give 3.6 g of product, 57% yield.

¹H NMR (500 MHz, CDCl₃ 5.21-5.11 (m, 1H), 5.08-5.07 (m, 1H), 4.08-4.02 (m, 1H), 3.88-3.85 (m, 1H), 3.53-3.36 (m, 2H), 2.10-2.00 (m, 4H), 1.73-1.68(m, 7H), 1.60 (m, 3H), 1.28-1.21 (m, 1.5H), 1.18-1.09 (m, 1.5H), 0.98-0.96 (m, 2H), 0.74-0.70 (m, 2H).

Propionamide, N-Cyclopropylmethyl-N-[2,6-nonadienyl]-(2E,6Z)

To a reaction flask under nitrogen, NaH (2.3 g, 56 mmol) and 100 mL of THF were charged. The reaction was heated to 50° C., and amide (10.0 g, 50 mmol) was fed in over 45 minutes. The mixture was aged for 1 hour, then bromomethylcyclopropane (11 g, 80 mmol) was fed in to the reaction over 15 minutes. The reaction was allowed to age for 4 hours, and was then quenched with 75 mL of water. The layers were separated and the organic lasyer was washed with saturated NaHCO₃ solution, water, and brine. The solvent was removed under reduced pressure. The product was purified by silica gel chromatography eluting with (0-50% EtOAc/hexanes) to give 6.2 g of product, 48% yield.

¹H NMR (500 MHz, CDCl₃ 5.58-5.52 (m, 1H), 5.42-5.33 (m, 2H), 5.30-5.27 (m, 1H), 4.05 (d, J=6.12 Hz, 0.8H), 3.92 (d, J=4.97 Hz, 1.2H), 3.24 (d, J=6.8 Hz, 1.2H), 3.13 (d, J=6.5 Hz, 0.8H), 2.38 (q, J=7.4 Hz, 0.8H), 2.33 (q, J=7.4 Hz, 1.2H), 2.10 (bs, 4H), 2.02 (m, 2H), 1.16 (t, J=7.4 Hz, 1.2H), 1.14 (t, J=7.4 Hz, 1.8H), 0.95 (t, J=7.5 Hz, 3H), 1.0-0.93 (m, 0.4H), 0.93-0.84 (m, 0.6H), 0.57-0.53 (m, 0.8H), 0.49-0.45 (m, 1.2H), 0.23-0.18 (m, 2H).

EXAMPLE 9

Standard reduction processes of nitriles as described above and disclosed in commonly assigned U.S. application Ser. No. 11/154,399 filed Jun. 17, 2005 were used to prepare specific amine precursors of compounds described by the NMR data set forth below:

Cyclopropanecarboxamide, N-[[2-Methyl-2-(4-methyl-3-pentenyl)cyclopropyl]methyl]-

To a reaction flask under nitrogen, 1-[2-methyl-2-(4-methylpent-3-en-1-yl)cyclopropyl]methanamine (10.0 g, 0.06 mol), triethylamine (10.4 mL, 0.07 mol), and 75 ml of anhydrous methylene chloride. The reaction was cooled to −5° C. and cyclopropane carboxylic acid chloride (6.9 g, 0.066 mol) was feed in dropwise. Once the feed was complete the reaction mixture was aged for 3 hours at room temperature before quenching with 75 mL of water. The organic was extracted and washed with brine. Kugelrohr distillation afforded 8.1 g of product, 57% yield.

¹H NMR (500 MHz, CDCl₃) δ: 0.08-0.16 (m, 1H), 0.46-0.51 (m, 1H), 0.77-0.98 (m, 5H), 1.05-1.09 (2s, 3H), 1.11-1.18 (m, 1H), 1.26-1.40 (m, 2H), 1.61-1.74 (m, 6H), 2.01-2.17 (m, 2H), 3.33 (br. s, 2H), 5.10 (m, 1H), 5.58 (br. s, 1H).

Acetamide, N-[[2-methyl-2-(4-methyl-3-pentenyl)cyclopropyl]methyl]-

Acetyl Chloride 1.1 eq, 1-[2-methyl-2-(4-methylpent-3-en-1-yl)cyclopropyl]methanamine 1.0 eq, triethylamine 1.2 eq, quenched with water yield 65% yield.

¹H NMR (500 MHz, CDCl₃) δ: 0.09-0.13 (m, 1H), 0.42-0.51 (m, 1H), 0.72-0.79 (m, 1H), 1.05-1.07 (2s, 3H), 1.09 & 1.43 (m, 3H), 1.62 (s, 3H), 1.69 (s, 3H), 1.98 (s, 3H), 2.01-2.09 (m, 2H), 3.11-3.36 (m, 2H), 5.08-5.11 (m, 1H), 5.41 (br. s., 1H).

Propanamide, N-[[2-methyl-2-(4-methyl-3-pentenyl)cyclopropyl]methyl]-

Propionyl chloride 1.1 eq, 1-[2-methyl-2-(4-methylpent-3-en-1-yl)cyclopropyl]methanamine 1.0 eq, triethylamine 1.2 eq, quenched with water yield 62% yield.

¹H NMR (500 MHz, CDCl₃) δ: 0.09-0.14 (m, 1H), 0.45-0.51 (m, 1H), 0.73-0.79 (m, 1H), 1.05-1.07 (2s, 3H), 1.09-1.14 & 1.31-1.39 (m, 3H), 1.17 (t, J=7.55 Hz, 3H), 1.61 (s, 3H), 1.68 (s, 3H), 2.04-2.09 (m, 2H), 2.20 (q, J=7.57 Hz, 2H), 3.11-3.86 (m, 2H), 5.08-5.12 (m, 1H), 5.38 (m, 1H).

The reaction sequence according to Example 2 was used to prepare specific compounds described by the NMR data set forth below:

IsoPropanamide, N-[[2-methyl-2-(4-methyl-3-pentenyl)cyclopropyl]methyl]-2-methyl-

Isobutyric anhydride 1.1 eq, 1-[2-methyl-2-(4-methylpent-3-en-1-yl)cyclopropyl]methanamine 1.0 eq, triethylamine 1.2 eq, quenched with water yield 70% yield.

¹H NMR (500 MHz, CDCl₃) δ: 0.10-0.14 (m, 1H), 0.45-0.51 (m, 1H), 0.73-0.79 (m, 1H), 1.05-1.07 (2s, 3H), 1.09-1.13 & 1.31-1.39 (m, 3H), 1.16 (d, J=6.89 Hz, 6H), 1.61 (s, 3H), 1.68 (s, 3H), 2.01-2.10 (m, 2H), 2.34 (septet, J=6.89 Hz, 1H), 3.09-3.86 (m, 2H), 5.08-5.12 (m, 1H), 5.39 (br. s., 1H).

2-butenamide, N-[[2-methyl-2-(4-methyl-3-pentenyl)cyclopropyl]methyl]-

Crotonic anhydride 1.1 eq, 1-[2-methyl-2-(4-methylpent-3-en-1-yl)cyclopropyl]methanamine 1.0 eq, triethylamine 1.2 eq, quenched with water yield 61% yield.

¹H NMR (500 MHz, CDCl₃) δ: 0.10-0.15 (m, 1H), 0.45-0.51 (m, 1H), 0.75-0.82 (m, 1H), 1.05-1.08 (2s, 3H), 1.10-1.15 (m, 1H), 1.3-1.39 (m, 1H), 1.61 (s, 3H), 1.68 (s, 3H), 1.85 (d, J=6.8 Hz, 3H), 2.02-2.09 (m, 2H), 3.17-3.44 (m, 2H), 5.08-5.12 (m, 1H), 5.36 (br. s, 1H), 5.79 (d, J=15.2 Hz, 1H), 6.83 (dq, J=15.1, 6.9 Hz, 1H).

EXAMPLE 10

The reaction sequence according to Example 2, where R1-R7 have the same meaning as set forth in structure 5, was used to prepare specific compounds described by the NMR data set forth below:

2-methyl-2-(4-methyl-3-pentenyl)Cyclopropanecarboxamide, N-cyclopropyl-

2-methyl-2-(4-methylpent-3-en-1-yl)cyclopropanecarboxylic acid (20.0 g, 0.11 mol) in 150 mL of ethyl acetate and ethylchloroformate (17.9 g, 0.165 mol) were charged to a reaction flask. The reaction mixture was then cooled to 0° C. Triethylamine (23.8 g, 0.165 mol) was slowly added while maintaining the reaction temperature at 0° C. Once the feed was complete the reaction mixture was aged for 2 hours. Next, cyclopropylamine (18.8 g, 0.33 mol) was slowly added over 1 hour. Once the feed was complete the reaction mixture was allowed to warm to room temperature and aged for 2 hours. The reaction mixture was then quenched with 200 mL of water, extracted with diethyl ether and washed with brine. Kugelrohr distillation afforded 15.1 g of the product, 62% yield.

¹H NMR (500 MHz, CDCl₃) δ: 0.44-0.90 (m, 6H), 1.06 (t, 1H, J=4.77 Hz) 1.1 & 1.14 (2s, 3H), 1.16-1.43 (m, 2H), 1.60-1.70 (m, 6H), 2.01-2.13 (m, 2H), 2.68-2.75 (m, 1H), 5.09 (br. s, 1H), 5.45-5.64 (m, 1H).

2-methyl-2-(4-methyl-3-pentenyl) Cyclopropanecarboxamide, N,N-dimethyl-

Dimethylamine 3.0 eq, 2-[(3Z)-hex-3-en-1-yl]cyclopropanecarboxylic acid 1.0 eq, ethylchloroformate 2.0 eq, triethylamine 2.0 eq, quenched with saturated sodium chloride solution, 55% yield.

¹H NMR (500 MHz, CDCl₃) δ: 0.61 (m, 1H), 0.95 (t, J=7.52 Hz, 3H), 0.96 (m, 1H), 1.17 (m, 1H), 1.37 (m, 2H), 1.49 (m, 2H), 2.04 (p, J=7.16 Hz, 2H), 2.14 (q, J=6.69 Hz, 2H), 2.95 (s, 3H), 3.15 (s, 3H), 5.30-5.49 (m, 2H).

2-methyl-2-(4-methyl-3-pentenyl) Cyclopropanecarboxamide, N-ethyl-

Ethylamine 3.0 eq, 2-methyl-2-(4-methylpent-3-en-1-yl)cyclopropanecarboxylic acid 1.0 eq, ethylchloroformate 2.0 eq, triethylamine 2.0 eq was quenched with saturated sodium chloride solution to give a 63% yield.

¹H NMR (500 MHz, CDCl₃) δ: 0.70 (m, 1H), 1.12-1.70 (m, 16 H), 1.92-2.20 (m, 2H), 3.30 (m, 2H), 5.08-5.11 (m, 1H), 5.49-5.52 (m, 1H).

2-methyl-2-(4-methyl-3-pentenyl) Cyclopropanecarboxamide, N-2-methylpropanyl-

Isobutylamine 3.0 eq, 2-methyl-2-(4-methylpent-3-en-1-yl)cyclopropanecarboxylic acid 1.0 eq, ethylchloroformate 2.0 eq, triethylamine 2.0 eq was quenched with saturated sodium chloride solution to give a 71% yield.

¹H NMR (500 MHz, CDCl₃) δ: 0.71 (br. s. 1H), 0.92 (d, J=6.43 Hz, 6H), 1.06 (m, 1H), 1.121.14 (2s, 3H), 0.19-1.26 (m, 2H), 1.39-1.44 (m, 1H), 1,61 (2s, 3H), 1.69 (2s, 3H), 1.74-1.82 (m, 1H), 1.93-2.13 (m, 2H), 3.11 (br. s, 2H), 5.09-5.12 (m, 1H), 5.54 (br. s, 1H).

2-methyl-2-(4-methyl-3-pentenyl) Cyclopropanecarboxamide, N-methyl-

Methylamine 3.0 eq, 2-methyl-2-(4-methylpent-3-en-1-yl)cyclopropanecarboxylic acid 1.0 eq, ethylchloroformate 2.0 eq, triethylamine 2.0 eq was quenched with saturated sodium chloride solution to 51% yield.

¹H NMR (500 MHz, CDCl₃) δ: 0.70-0.72 & 1.05-1.07 (m, 1H), 1.11-1.15 (2s, 3H), 1.17-1.26 & 1.27-1.43 (m, 2H), 1.59-1.70 (m, 7H), 1.906-2.13 (m, 2H), 2.82 (s, 3H), 5.06-5.11 (m, 1H), 5.25-5.32 & 5.49 (m, 1H).

2-methyl-2-(4-methyl-3-pentenyl) Cyclopropanecarboxamide, N-2-propenyl-

Allylamine 3.0 eq, 2-methyl-2-(4-methylpent-3-en-1-yl)cyclopropanecarboxylic acid 1.0 eq, ethylchloroformate 2.0 eq, triethylamine 2.0 eq was quench with saturated sodium chloride solution to produce a 72% yield.

¹H NMR (500 MHz, CDCl₃) δ: 0.71-0.74 (m, 1H), 0.84-0.90 (m, ˜38% of 1H) 1.08(t, ˜62% of 1H, J=4.87 Hz), 1.12-1.15 (2s, 3H), 1.21-1.28 (m, 2H), 1.41-1.50 (m, 1H), 1.55-1.69 (m, 6H), 1.95-2.14 (m, 2H), 3.88-3.93 (m, 2H), 5.08-5.14 (m, 2H), 5.17-5.22 (m, 1H), 5.53-5.66 (m, 1H), 5.81-5.92 (m, 1H).

2-methyl-2-(4-methyl-3-pentenyl) Cyclopropanecarboxamide, N-1-methylethyl-

Isopropyl amine 3.0 eq, 2-methyl-2-(4-methylpent-3-en-1-yl)cyclopropanecarboxylic acid 1.0 eq, ethylchloroformate 2.0 eq, triethylamine 2.0 eq was quenched with saturated sodium chloride solution to provide a 68% yield.

¹H NMR (500 MHz, CDCl₃) δ: 0.65-0.69 & 1.03-1.04 (m, 1H), 1.11-1.30 (n, 12H), 1.39-1.46 & 1.46-1.51 (m, 1H), 1.59-1.71 (m, 6 H), 1.94-2.10 (m, 2H), 4.06-4.11 (m, 1H), 5.08-5.12 (m, 1H), 5.29-5.33 (m, 1H).

EXAMPLE 11

A consumer panel trained in basic taste for ranking of intensity and quality of the basic taste attribute were asked to compare Umami strength of solutions of MSG, Ribotides, a commercially available blend of disodium guanylate and disodium inosinate and molecules of this invention.

A 440 mg Sodium broth base was used as the reference and testing was done according to the following protocol.

Objectives:

-   -   Evaluate molecules against extra salt, MSG, and Ribo in the         Chicken Broth base for the 4 attributes (Umami intensity, 1         Saltiness     -   Sweetness, and Bitterness.

Procedures:

-   -   Judges will rate each sample in set 1 for the intensity of         Saltiness, Sweetness, Bitterness, and Umami intensity using 1         Compusense.

Judges will repeat the same procedures for the 2 samples in set 2 (Replicate of set 1). Code Base Extra Ingredients Amount Needed Sample Set 1 1 392 Chicken Broth 0 0.5 Liter Base* 2 575 Chicken Broth 0.44% Salt 0.5 Liter Base* 3 400 Chicken Broth 0.65% MSG 0.5 Liter Base* 4 543 Chicken Broth 0.068% Ribo 0.5 Liter Base* 5 510 Chicken Broth 1 ppm J 0.5 Liter Base* 6 123 Chicken Broth 2 ppm J 0.5 Liter Base* Sample Set 2 1 528 Chicken Broth 0 0.5 Liter Base* 2 373 Chicken Broth 0.44% Salt 0.5 Liter Base* 3 768 Chicken Broth 0.65% MSG 0.5 Liter Base* 4 538 Chicken Broth 0.068% Ribo 0.5 Liter Base* 5 943 Chicken Broth 1 ppm J 0.5 Liter Base* 6 341 Chicken Broth 2 ppm J 0.5 Liter Base* *Chicken Broth Base (440 mg Na/Serving) = 1% Chicken Broth Powder #3422 + 0.35% Salt + 0.14% MSG + 0.02% Ribo **Set 2 is a Replicate of Set 1

The results showed that addition of 2 ppm of the prefered molecules of the invention added about the same intensity of additional Umami character as addition of an additional 0.5% salt, or 0.65% MSG or 0.08% ribotides. 

1-27. (canceled)
 28. The combination of claim 25 provided foodstuff, beverage, chewing gum, medicinal product, or toothpaste at a level greater than about 50 parts per billion.
 29. A N-substituted unsaturated alkyl amide compound having the structure selected from the group consisting of structure 3 and structure 4:

where R¹=H or methyl; R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl and methylene; R³ is selected from the group consisting of H, C₁-C₈ straight or branched chain alkyl, alkenyl, dienalkyl and phenyl; or if R¹=H, R² and R³ taken together can represent

 cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or cyclohexenyl; or if R¹=Me, R² and R³ taken together can represent

 or cyclopropyl, R⁴ is selected from the group consisting of C₁-C₄ alkyl, alkenyl; removed methylene R⁵ is selected from the group consisting of H, methyl or ethyl; R⁶ is selected from the group consisting of H, methyl and ethyl; R⁷ is selected from the group consisting of H, C₁-C₉ straight or branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no more than one ring; except for in the case of structure 3 when if R⁵=H or methyl and R⁶=H or methyl, R⁷ as described above and phenyl.
 30. A foodstuff comprising greater than about 50 parts per billion by weight of the compound of claim
 29. 31. In combination, a consumable material selected from the group consisting of beverages, foodstuff, chewing gum, dental and oral hygiene products; and an organoleptically acceptable level of the compound of claim
 29. 32. The combination of claim 31 wherein the level of the organoleptically acceptable compound is greater than about 50 parts per billion.
 33. The combination of claim 31 wherein the level of the organoleptically acceptable compound is provided at a level of from about 0.01 parts per million to about 50 parts per million by weight.
 34. A method of enhancing the salty taste of salt-containing beverages, foodstuff, chewing gum, dental and oral hygiene products which comprises adding a salt enhancing level of the structure selected from the group consisting of structure 3 and structure 4:

where R¹=H or methyl; R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl and methylene; R³ is selected from the group consisting of H, C₁-C₈ straight or branched chain alkyl, alkenyl, dienalkyl and phenyl; or if R¹=H, R² and R³ taken together can represent

 cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or cyclohexenyl; or if R¹=Me, R² and R³ taken together can represent

 or cyclopropyl, R⁴ is selected from the group consisting of C₁-C₄ alkyl, alkenyl; removed methylene R⁵ is selected from the group consisting of H, methyl or ethyl; R⁶ is selected from the group consisting of H, methyl and ethyl; R⁷ is selected from the group consisting of H, C₁-C₉ straight or branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no more than one ring; except for in the case of structure 3 when if R⁵=H or methyl and R⁶=H or methyl, R⁷ as described above and phenyl.
 35. The combination comprising: (a) the compound used in the method of claim 34; (b) and a foodstuff.
 36. The combination of claim 35 wherein the compound of claim 34 is described by structure
 3. 37. An organoleptically acceptable combination comprising (a) the compound used in the method of claim 34; (b) a second salt taste enhancing material; wherein the weight ratio of (a) to (b) is from about 1 to 10 from about 10 to
 1. 38. The combination of claim 37 wherein the weight ratio of (a) to (b) ranges from about 1 to 5 from about 5 to
 1. 39. The combination of claim 37 wherein the ratio of (a) to (b) ranges from about 1 to 3 to about 3 to
 1. 40. A process for augmenting, enhancing or imparting an umami taste to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage or soup comprising the step of adding to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage or soup an organoletically acceptable level of the compound used in the method of claim
 34. 41. The process of claim 40 wherein the level of the organoleptically acceptable level is greater than about 50 parts per billion by weight.
 42. A N-substituted unsaturated alkyl amide compound having the structure:

where R¹=H or methyl; R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl and methylene; R³ is selected from the group consisting of H, C₁-C₈ straight or branched chain alkyl, alkenyl, dienalkyl and phenyl; or if R¹=H, R² and R³ taken together can represent

 cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or cyclohexenyl; or if R¹=Me, R² and R³ taken together can represent

 or cyclopropyl, R⁴ is selected from the group consisting of C₁-C₄ alkyl; R⁵ is selected from the group consisting of H, methyl or ethyl; R⁶ is selected from the group consisting of H, methyl and ethyl; R⁷ is selected from the group consisting of H, C₁-C₉ straight or branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no more than one ring; except for in the case of structure 4 when if R⁵=H or methyl and R⁶=H or methyl, R⁷ as described above and phenyl.
 43. A foodstuff comprising greater than about 50 parts per billion by weight of the compound of claim
 42. 44. In combination, a consumable material selected from the group consisting of beverages, foodstuff, chewing gum, dental and oral hygiene products; and an organoleptically acceptable level of the compound of claim
 42. 45. The combination of claim 44 wherein the level of the organoleptically acceptable compound is greater than about 50 parts per billion.
 46. The combination of claim 44 wherein the level of the organoleptically acceptable compound is provided at a level of from about 0.01 parts per million to about 50 parts per million by weight.
 47. A method of enhancing the salty taste of salt-containing beverages, foodstuff, chewing gum, dental and oral hygiene products which comprises adding a salt enhancing level of the structure:

where R¹=H or methyl; R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl and methylene; R³ is selected from the group consisting of H, C₁-C₈ straight or branched chain alkyl, alkenyl, dienalkyl and phenyl; or if R¹=H, R² and R³ taken together can represent

 cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or cyclohexenyl; or if R¹=Me, R² and R³ taken together can represent

 or cyclopropyl, R⁴ is selected from the group consisting of C₁-C₄ alkyl; R⁵ is selected from the group consisting of H, methyl or ethyl; R⁶ is selected from the group consisting of H, methyl and ethyl; R⁷ is selected from the group consisting of H, C₁-C₉ straight or branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no more than one ring; except for in the case of structure 4 when if R⁵=H or methyl and R⁶=H or methyl, R⁷ as described above and phenyl.
 48. The combination comprising: (a) the compound used in the method of claim 47; (b) and a foodstuff.
 49. An organoleptically acceptable combination comprising (a) the compound used in the method of claim 47; (b) a second salt taste enhancing material; wherein the weight ratio of (a) to (b) is from about 1 to 10 from about 10 to
 1. 50. The combination of claim 47 wherein the weight ratio of (a) to (b) ranges from about 1 to 5 from about 5 to
 1. 51. The combination of claim 47 wherein the ratio of (a) to (b) ranges from about 1 to 3 to about 3 to
 1. 52. A process for augmenting, enhancing or imparting an umami taste to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage or soup comprising the step of adding to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage or soup an organoletically acceptable level of the compound used in the method of claim
 47. 53. The process of claim 52 wherein the level of the organoleptically acceptable level is greater than about 50 parts per billion by weight.
 54. A foodstuff or beverage containing wherein the salt or umami taste enhancer (a) is selected from the group consisting of: 2-butenamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-, (2E)-2-butenamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-, (2E)-2-butenamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-3-methyl-2-butenamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-3-methyl-2-butenamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-2-methyl-(2E)-2-butenamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-2-methyl-(2E)-Cyclopropanecarboxamide, N-[(2Z,6Z)-2,6-nonadienyl]-Cyclopropanecarboxamide, N-[(2E,6Z)-2,6-nonadienyl]-Cyclopropanecarboxamide, N-[(2E)-3-(3-cyclohexen-1-yl)-2-propenyl]-Cyclopropanecarboxamide, N-[(2E,6Z)-2,6-dodecadienyl]-Cyclopropanecarboxamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-Cyclopropanecarboxamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-Propanamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-2-methyl-Propanamide, N-[(2Z)-3,7-dimethyl-2,6-octadienyl]-2-methyl-Acetamide, N-[(2Z,6Z)-2,6-nonadienyl]-Acetamide, N-[(2E,6Z)-2,6-nonadienyl]-Acetamide, N-[(2Z,6Z)-2-methyl-2,6-nonadienyl]-Acetamide, N-[(2Z,6Z)-2-methyl-2,6-nonadienyl]-Cyclopropanecarboxamide, N-[[2-methyl-2-(4-methyl-3-pentenyl)cyclopropyl]methyl]-Acetamide, N-[[2-methyl-2-(4-methyl-3-pentenyl)cyclopropyl]methyl]-Cyclopropanecarboxamide, N-methyl-N-[(2E,6Z)-2,6-nonadienyl]-Cyclopropanecarboxamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-N-methyl- Cyclopropanecarboxamide, N-[(2E)-3,7-dimethyl-2,6-octadienyl]-N-ethyl-Propanamide, N-[(2E,6Z)-2,6-nonadienyl]-N-cyclopropylmethyl-N,N,3,7-Tetramethylocta-2,6-dienamide,(2E)-2-propenamide, 3-(3-cyclohexen-1-yl)-N-ethyl-,(2E)-3,7-dimethyl-2,6-octadienamide, N-ethyl-,(2E)-2,6-nonadienamide, N,N-dimethyl-, (2E,6Z)-2,6-nonadienamide, N-cyclopropyl, 2-methyl-, (2E,6Z)—-2,6-dodecadienamide, N-ethyl-, (2E,6Z)-2,6-nonadienamide, N-cyclopropyl-, (2E,6Z)-2,6-nonadienamide, N-ethyl-, (2E,6Z)-.
 55. A N-substituted unsaturated alkyl amide compound having the structure selected from the group consisting of structure 1 and structure 2:

where R¹=H or methyl; R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl and methylene; R³ is selected from the group consisting of H, C₁-C₈ straight or branched chain alkyl, alkenyl, dienalkyl and phenyl; or if R¹=H, R² and R³ taken together can represent

 cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or cyclohexenyl; or if R¹=Me, R² and R³ taken together can represent

 or cyclopropyl, R⁴ is selected from the group consisting of H, methyl or ethyl; R⁵ is selected from the group consisting of H, methyl and ethyl; R⁶ is selected from the group consisting of H, C₁-C₉ straight or branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no more than one ring; with the proviso that in structure 1 when R⁴ is H or methyl; and R⁵ is H or methyl, R⁶ may be selected from the group described above phenyl, and if R¹=H and R²=H, then R³ can not be H or methyl unless R⁴=R⁵=H.
 56. The compound of the formula

where R¹=H or methyl; R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl and methylene; R³ is selected from the group consisting of H, C₁-C₈ straight or branched chain alkyl, alkenyl, dienalkyl and phenyl; or if R¹=H, R² and R³ taken together can represent

 cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or cyclohexenyl; or if R¹=Me, R² and R³ taken together can represent

 or cyclopropyl, R⁴ is selected from the group consisting of H, methyl or ethyl; R⁵ is selected from the group consisting of H, methyl and ethyl; R⁶ is selected from the group consisting of H, C₁-C₉ straight or branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no more than one ring; with the proviso that in structure 1 when if R⁴ is H or methyl and R⁵ is H or methyl, R⁶ may be selected from the group described above and phenyl, and if R¹=H and R²=H, then R³ can not be H or methyl unless R⁴=R⁵=H.
 57. A foodstuff comprising greater than about 50 parts per billion by weight of the compound of claim
 55. 58. In combination, a consumable material selected from the group consisting of beverages, foodstuff, chewing gum, dental and oral hygiene products; and an organoleptically acceptable level of the compound of claim
 55. 59. The combination of claim 58 wherein the level of the organoleptically acceptable compound is greater than about 50 parts per billion.
 60. The combination of claim 58 wherein the level of the organoleptically acceptable compound is provided at a level of from about 0.01 parts per million to about 50 parts per million by weight.
 61. A method of enhancing the salty taste of salt-containing beverages, foodstuff, chewing gum, dental and oral hygiene products which comprises adding a salt enhancing level of the structure selected from the group consisting of structure 1 and structure 2:

where R¹=H or methyl; R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl and methylene; R³ is selected from the group consisting of H, C₁-C₈ straight or branched chain alkyl, alkenyl, dienalkyl and phenyl; if R¹=H, R² and R³ taken together can represent

 cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or cyclohexenyl; or if R¹=Me, R² and R³ taken together can represent

 or cyclopropyl, R⁴ is selected from the group consisting of H, methyl or ethyl; R⁵ is selected from the group consisting of H, methyl and ethyl; R⁶ is selected from the group consisting of H, C₁-C₉ straight or branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no more than one ring; with the proviso that in structure 1 when if R⁴ is H or methyl and R⁵=H or methyl, R⁶ may be selected from the group described above and phenyl, and if R¹=H and R²=H, then R³ can not be H or methyl unless R⁴=R⁵=H.
 62. The combination comprising: (a) the compound used in the method of claim 61; (b) and a foodstuff.
 63. The combination of claim 62 wherein the compound of claim 61 is described by structure
 1. 64. An organoleptically acceptable combination comprising (a) the compound used in the method of claim 61; (b) a second salt taste enhancing material; wherein the weight ratio of (a) to (b) is from about 1 to 10 from about 10 to
 1. 65. The combination of claim 64 wherein the weight ratio of (a) to (b) ranges from about 1 to 5 from about 5 to
 1. 66. The combination of claim 64 wherein the ratio of (a) to (b) ranges from about 1 to 3 to about 3 to
 1. 67. A process for augmenting, enhancing or imparting an umami taste to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage or soup comprising the step of adding to a foodstuff, chewing gum, medicinal product, toothpaste, alcoholic beverage, aqueous beverage or soup an organoletically acceptable level of the compound used in the method of claim
 61. 68. The process of claim 67 wherein the level of the organoleptically acceptable level is greater than about 50 parts per billion by weight.
 69. In combination an organoleptically acceptable amount of the compound having the structure selected from the group consisting of structure 1 and structure 2:

where R¹=H or methyl; R² is selected from the group consisting of H, C₁-C₄ alkyl, alkenyl and methylene; R³ is selected from the group consisting of H, C₁-C₈ straight or branched chain alkyl, alkenyl, dienalkyl and phenyl; if R¹=H, R² and R³ taken together can represent

 cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, or cyclohexenyl; or if R¹=Me, R² and R³ taken together can represent

 or cyclopropyl, R⁴ is selected from the group consisting of H, methyl or ethyl; R⁵ is selected from the group consisting of H, methyl and ethyl; R⁶ is selected from the group consisting of H, C₁-C₉ straight or branched chain alkyl, alkenyl, alkyldienyl, acyclic or containing no more than one ring; with the proviso that in structure 1 when if R⁴ is H or methyl and R⁵=H or methyl, R⁶ may be selected from the group described above and phenyl, and if R¹=H and R²=H, then R³ can not be H or methyl unless R⁴=R⁵=H.
 70. The combination of claim 69 containing an additional salt substitute compounds.
 71. The combination of claim 70 where the salt substitute compound is selected from the group consisting of potassium chloride, ribonucleotides, cationic amino acids, low molecular weight dipeptides, monosodium glutamates and yeasts.
 72. The combination of claim 71 wherein the salt substitute compound is selected from the group consisting of arginine hydrochloride, arginine ammonium chloride, lysine hydrochloride and lysine-ornithine hydrochloride.
 73. The combination of claim 70 provided to a foodstuff, beverage, chewing gum, medicinal product, or toothpaste at a level of greater than 50 parts per billion. 